Home Cart 0 Sign in  
X

[ CAS No. 951884-54-1 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
3d Animation Molecule Structure of 951884-54-1
Chemical Structure| 951884-54-1
Chemical Structure| 951884-54-1
Structure of 951884-54-1 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 951884-54-1 ]

Related Doc. of [ 951884-54-1 ]

Alternatived Products of [ 951884-54-1 ]
Product Citations

Product Details of [ 951884-54-1 ]

CAS No. :951884-54-1 MDL No. :MFCD09800997
Formula : C8H12ClN3S Boiling Point : -
Linear Structure Formula :- InChI Key :UFIHRHMWSNBGPR-UHFFFAOYSA-N
M.W : 217.72 Pubchem ID :26370202
Synonyms :

Calculated chemistry of [ 951884-54-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 57.68
TPSA : 63.11 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.41 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.45
Log Po/w (XLOGP3) : 3.13
Log Po/w (WLOGP) : 2.48
Log Po/w (MLOGP) : 1.6
Log Po/w (SILICOS-IT) : 2.2
Consensus Log Po/w : 2.37

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.31
Solubility : 0.108 mg/ml ; 0.000495 mol/l
Class : Soluble
Log S (Ali) : -4.12
Solubility : 0.0163 mg/ml ; 0.0000751 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -3.65
Solubility : 0.049 mg/ml ; 0.000225 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.22

Safety of [ 951884-54-1 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:
Recommend Products
Same Skeleton Products

Technical Information

• 1,4-Addition of an Amine to a Conjugated Enone • 1,4-Addition of an Amine to a Conjugated Enone • Acid-Catalyzed α -Halogenation of Ketones • Addition of a Hydrogen Halide to an Internal Alkyne • Alcohols from Haloalkanes by Acetate Substitution-Hydrolysis • Alkyl Halide Occurrence • Alkylation of an Alkynyl Anion • Amides Can Be Converted into Aldehydes • Amine Synthesis from Nitriles • Amine Synthesis from Nitriles • Amines Convert Acyl Chlorides into Amides • Amines Convert Esters into Amides • An Alkane are Prepared from an Haloalkane • Azide Reduction by LiAlH4 • Azide Reduction by LiAlH4 • Basicity of Amines • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chan-Lam Coupling Reaction • Chichibabin Reaction • Chloroalkane Synthesis with SOCI2 • Convert Haloalkanes into Alcohols by SN2 • Diazotization Reaction • DIBAL Attack Nitriles to Give Ketones • Dithioacetal Formation • Enamine Formation • Formation of an Amide from an Amine and a Carboxylic Acid • Formation of an Amide from an Amine and a Carboxylic Acid • Friedel-Crafts Alkylation of Benzene with Haloalkanes • General Reactivity • Grignard Reaction • Halogenation of Alkenes • Hemiaminal Formation from Amines and Aldehydes or Ketones • Hemiaminal Formation from Amines and Aldehydes or Ketones • Hiyama Cross-Coupling Reaction • Hofmann Elimination • Hofmann Rearrangement • Hydride Reductions • Hydrolysis of Imines to Aldehydes and Ketones • Imine Formation from Amines and Aldehydes or Ketones • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Leuckart-Wallach Reaction • Mannich Reaction • Methylation of Ammonia • Methylation of Ammonia • Nitrosation of Amines • Nucleophilicity of Sulfur Compounds • Oxidation States of Sulfur Compounds • Peptide Bond Formation with DCC • Petasis Reaction • Preparation of Amines • Preparation of LDA • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reduction of an Amide to an Amine • Reduction of an Amide to an Amine • Reduction of Disulfides to Thiols • Reductive Amination • Reductive Amination • Ring Opening of Azacyclopropanes • Ring Opening of Azacyclopropanes • Ring Opening of Oxacyclobutanes • Specialized Acylation Reagents-Vilsmeier Reagent • Stille Coupling • Strecker Synthesis • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Synthesis of 2-Amino Nitriles • Thioacetals May Be Hydrolyzed to Carbonyl Compounds • Ugi Reaction
Historical Records

Related Functional Groups of
[ 951884-54-1 ]

Chlorides

Chemical Structure| 951884-05-2

[ 951884-05-2 ]

6-Chloro-N-cyclopropyl-2-(methylthio)pyrimidin-4-amine

Similarity: 0.95

Chemical Structure| 261765-64-4

[ 261765-64-4 ]

6-Chloro-2-(methylthio)-N-propylpyrimidin-4-amine

Similarity: 0.94

Chemical Structure| 1289386-63-5

[ 1289386-63-5 ]

6-Chloro-N-isopropyl-2-(methylsulfinyl)pyrimidin-4-amine

Similarity: 0.88

Chemical Structure| 1261229-62-2

[ 1261229-62-2 ]

6-Chloro-2-(methylthio)-N-(pyrrolidin-3-yl)pyrimidin-4-amine hydrochloride

Similarity: 0.87

Chemical Structure| 478258-67-2

[ 478258-67-2 ]

6-Chloro-N-methyl-2-(methylthio)pyrimidin-4-amine

Similarity: 0.87

Amines

Chemical Structure| 951884-05-2

[ 951884-05-2 ]

6-Chloro-N-cyclopropyl-2-(methylthio)pyrimidin-4-amine

Similarity: 0.95

Chemical Structure| 261765-64-4

[ 261765-64-4 ]

6-Chloro-2-(methylthio)-N-propylpyrimidin-4-amine

Similarity: 0.94

Chemical Structure| 1289386-63-5

[ 1289386-63-5 ]

6-Chloro-N-isopropyl-2-(methylsulfinyl)pyrimidin-4-amine

Similarity: 0.88

Chemical Structure| 1261229-62-2

[ 1261229-62-2 ]

6-Chloro-2-(methylthio)-N-(pyrrolidin-3-yl)pyrimidin-4-amine hydrochloride

Similarity: 0.87

Chemical Structure| 478258-67-2

[ 478258-67-2 ]

6-Chloro-N-methyl-2-(methylthio)pyrimidin-4-amine

Similarity: 0.87

Sulfides

Chemical Structure| 951884-05-2

[ 951884-05-2 ]

6-Chloro-N-cyclopropyl-2-(methylthio)pyrimidin-4-amine

Similarity: 0.95

Chemical Structure| 261765-64-4

[ 261765-64-4 ]

6-Chloro-2-(methylthio)-N-propylpyrimidin-4-amine

Similarity: 0.94

Chemical Structure| 1261229-62-2

[ 1261229-62-2 ]

6-Chloro-2-(methylthio)-N-(pyrrolidin-3-yl)pyrimidin-4-amine hydrochloride

Similarity: 0.87

Chemical Structure| 478258-67-2

[ 478258-67-2 ]

6-Chloro-N-methyl-2-(methylthio)pyrimidin-4-amine

Similarity: 0.87

Related Parent Nucleus of
[ 951884-54-1 ]

Pyrimidines

Chemical Structure| 951884-05-2

[ 951884-05-2 ]

6-Chloro-N-cyclopropyl-2-(methylthio)pyrimidin-4-amine

Similarity: 0.95

Chemical Structure| 261765-64-4

[ 261765-64-4 ]

6-Chloro-2-(methylthio)-N-propylpyrimidin-4-amine

Similarity: 0.94

Chemical Structure| 1289386-63-5

[ 1289386-63-5 ]

6-Chloro-N-isopropyl-2-(methylsulfinyl)pyrimidin-4-amine

Similarity: 0.88

Chemical Structure| 1261229-62-2

[ 1261229-62-2 ]

6-Chloro-2-(methylthio)-N-(pyrrolidin-3-yl)pyrimidin-4-amine hydrochloride

Similarity: 0.87

Chemical Structure| 478258-67-2

[ 478258-67-2 ]

6-Chloro-N-methyl-2-(methylthio)pyrimidin-4-amine

Similarity: 0.87

; ;