[ CAS No. 1314538-55-0 ] {[proInfo.proName]}

Name: 1314538-55-0|Potassium (((tert-butoxycarbonyl)amino)methyl)trifluoroborate|95%
Brand: Ambeed
SKU: A139380
Price: 5.0 USD
Availability: InStock
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Structure of 1314538-55-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1314538-55-0 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 1314538-55-0 ]

SDS Specification

Alternatived Products of [ 1314538-55-0 ]

Product Details of [ 1314538-55-0 ]

CAS No. :	1314538-55-0	MDL No. :	MFCD19686142
Formula :	C₆H₁₂BF₃KNO₂	Boiling Point :	-
Linear Structure Formula :	-	InChI Key :	WSOSBCPWIQUNLD-UHFFFAOYSA-N
M.W :	237.07	Pubchem ID :	53483531
Synonyms :

Calculated chemistry of [ 1314538-55-0 ]

Physicochemical Properties

Num. heavy atoms :	14
Num. arom. heavy atoms :	0
Fraction Csp3 :	0.83
Num. rotatable bonds :	5
Num. H-bond acceptors :	5.0
Num. H-bond donors :	1.0
Molar Refractivity :	43.49
TPSA :	38.33 Å²

Pharmacokinetics

GI absorption :	High
BBB permeant :	Yes
P-gp substrate :	No
CYP1A2 inhibitor :	No
CYP2C19 inhibitor :	No
CYP2C9 inhibitor :	No
CYP2D6 inhibitor :	No
CYP3A4 inhibitor :	No
Log Kp (skin permeation) :	-5.99 cm/s

Lipophilicity

Log Po/w (iLOGP) :	0.0
Log Po/w (XLOGP3) :	2.48
Log Po/w (WLOGP) :	3.16
Log Po/w (MLOGP) :	1.32
Log Po/w (SILICOS-IT) :	-0.19
Consensus Log Po/w :	1.35

Druglikeness

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

Water Solubility

Log S (ESOL) :	-2.54
Solubility :	0.68 mg/ml ; 0.00287 mol/l
Class :	Soluble
Log S (Ali) :	-2.93
Solubility :	0.279 mg/ml ; 0.00118 mol/l
Class :	Soluble
Log S (SILICOS-IT) :	-2.12
Solubility :	1.79 mg/ml ; 0.00753 mol/l
Class :	Soluble

Medicinal Chemistry

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

Safety of [ 1314538-55-0 ]

Signal Word:	Warning	Class:	N/A
Precautionary Statements:	P261-P305+P351+P338	UN#:	N/A
Hazard Statements:	H302-H315-H319-H335	Packing Group:	N/A
GHS Pictogram:

Application In Synthesis of [ 1314538-55-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Upstream synthesis route of [ 1314538-55-0 ]
Downstream synthetic route of [ 1314538-55-0 ]

[ 1314538-55-0 ] Synthesis Path-Upstream 1~10

1
[ 623-03-0 ]
[ 1314538-55-0 ]
[ 66389-80-8 ]

Reference： [1] Organic Letters, 2011, vol. 13, # 15, p. 3956 - 3959

2
[ 1314538-55-0 ]
[ 66389-80-8 ]

Reference： [1] Organic Letters, 2013, vol. 15, # 10, p. 2534 - 2537

3
[ 1314538-55-0 ]
[ 138373-10-1 ]
[ 66389-80-8 ]

Reference： [1] Organic Letters, 2012, vol. 14, # 12, p. 3138 - 3141

4
[ 1314538-55-0 ]
[ 292638-85-8 ]
[ 85909-04-2 ]

Reference： [1] Advanced Synthesis and Catalysis, 2014, vol. 356, # 13, p. 2749 - 2755

5
[ 1314538-55-0 ]
[ 100-00-5 ]
[ 94838-58-1 ]

Reference： [1] Organic Letters, 2011, vol. 13, # 15, p. 3956 - 3959

6
[ 1142-27-4 ]
[ 1314538-55-0 ]
[ 94838-58-1 ]

Reference： [1] Organic Letters, 2013, vol. 15, # 10, p. 2534 - 2537

7
[ 1314538-55-0 ]
[ 104-88-1 ]
[ 156866-52-3 ]

Reference： [1] Organic Letters, 2011, vol. 13, # 15, p. 3956 - 3959

8
[ 1314538-55-0 ]
[ 69088-97-7 ]
[ 156866-52-3 ]

Reference： [1] Organic Letters, 2012, vol. 14, # 12, p. 3138 - 3141

9
[ 2905-65-9 ]
[ 1314538-55-0 ]
[ 180863-55-2 ]

Reference： [1] Organic Letters, 2011, vol. 13, # 15, p. 3956 - 3959

10
[ 24424-99-5 ]
[ 1314538-55-0 ]

Reference： [1] Organic Letters, 2011, vol. 13, # 15, p. 3956 - 3959