Home Cart Sign in  
Chemical Structure| 124845-04-1 Chemical Structure| 124845-04-1

Structure of 124845-04-1

Chemical Structure| 124845-04-1

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

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

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 124845-04-1 ]

CAS No. :124845-04-1
Formula : C7H7NO3
M.W : 153.14
SMILES Code : O=C(C1=C(C2CC2)ON=C1)O
MDL No. :MFCD06798100
InChI Key :KIJMAOMSRMPYIY-UHFFFAOYSA-N
Pubchem ID :14819892

Safety of [ 124845-04-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 124845-04-1 ]

* 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.

  • Downstream synthetic route of [ 124845-04-1 ]

[ 124845-04-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 32249-35-7 ]
  • [ 4637-24-5 ]
  • [ 124845-04-1 ]
YieldReaction ConditionsOperation in experiment
80.13% 1,1-Dimethoxy-N,N-dimethylmethanamine (1, 24g, 0.2 mol) andmethyl 3-cyclopropyl-3-oxo- propanoate (2, 28g, 0.2 mol) weremixed and heated for 20 h at 60 C. The obtained yellow oil wasfirstly dissolved in methanol (200 mL) and water (100 mL), andthen hydroxylamine hydrochloride (14g, 0.2 mol) was added. Thesolvents were evaporated under vacuum after the mixture washeated for 90 min at 60 C. The residuewas dissolved in the mixtureof acetic acid (100 mL) and concentrated HCl (100 mL) and refluxedfor 4h. The reaction mixture was diluted with water (500 mL) and extracted with ethyl acetate (200 mL 3). The organic layer wascombined and washed with brine, and then dried with anhydroussodium sulfate. Ethyl acetate was evaporated under vacuum. Theresidue was subjected to a silica gel column and eluted with themixture of ethyl acetate and petroleum ether at the ratio of 1:3 (v/v) to afford 3. Compound 3 was obtained as white solid (yield80.13%), mp, 163e165 C; 1H NMR (500 MHz, Chloroform-d): d 8.53(s, 1H), 2.91 (m, 1H), 1.38 (m, 2H), 1.3 (m, 2H). 13C NMR (126 MHz,Chloroform-d): d 179.91, 167.63, 150.62, 108.36, 10.86, 8.87. ESI-MS:m/z 152, [M H]-.
Methyl 3-cyclopropyl-3-oxopropanoate (0.28 g, 2 mmol) and 1,1-dimethoxy-N,N-dimethylmethanamine (0.24 g, 2 mmol) was mixed and heated for 20 h at 60 C. The bright yellow oil was dissolved in methanol (2 mL) and H2O (1 mL) and hydroxylamine hydrochloride (0.14 g, 2 mmol) was added, resulting in a pH of ca 5. The reaction was heated for 90 min at 60 C. The solvents were evaporated and the residue refluxed in acetic acid: conc. HCl (3+3 mL) for 4 h. The mixture was stored at room temperature for 2 days and the solid was filtered off and dried in vacuum to yield the title compound as a grey solid. This compound is also commercially available. 1H NMR (400 MHz, CHLOROFORM-D) δ ppm 1.18-1.28 (m, 2H) 1.28-1.35 (m, 2H) 2.78-2.90 (m, 1H) 8.45 (s, 1H)
 

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 124845-04-1 ]

Carboxylic Acids

Chemical Structure| 134541-04-1

A432102 [134541-04-1]

5-Propylisoxazole-4-carboxylic acid

Similarity: 0.94

Chemical Structure| 134541-05-2

A369499 [134541-05-2]

5-Isopropylisoxazole-4-carboxylic acid

Similarity: 0.94

Chemical Structure| 134541-06-3

A358207 [134541-06-3]

5-(tert-Butyl)isoxazole-4-carboxylic acid

Similarity: 0.93

Chemical Structure| 134541-03-0

A472038 [134541-03-0]

5-Ethylisoxazole-4-carboxylic acid

Similarity: 0.90

Chemical Structure| 134541-09-6

A239561 [134541-09-6]

5-(2-Carboxyethyl)isoxazole-4-carboxylic acid

Similarity: 0.89

Related Parent Nucleus of
[ 124845-04-1 ]

Isoxazoles

Chemical Structure| 134541-04-1

A432102 [134541-04-1]

5-Propylisoxazole-4-carboxylic acid

Similarity: 0.94

Chemical Structure| 134541-05-2

A369499 [134541-05-2]

5-Isopropylisoxazole-4-carboxylic acid

Similarity: 0.94

Chemical Structure| 134541-06-3

A358207 [134541-06-3]

5-(tert-Butyl)isoxazole-4-carboxylic acid

Similarity: 0.93

Chemical Structure| 134541-03-0

A472038 [134541-03-0]

5-Ethylisoxazole-4-carboxylic acid

Similarity: 0.90

Chemical Structure| 134541-09-6

A239561 [134541-09-6]

5-(2-Carboxyethyl)isoxazole-4-carboxylic acid

Similarity: 0.89