L-Vinylglycine hydrochloride

L-Vinylglycine hydrochloride Suppliers list
Company Name: Chembon Pharmaceutical Co., Ltd.  
Tel: 028-84252981 18583719936
Email: sales@chembon.com.cn
Company Name: Watson Biotechnology Co.,Ltd  
Tel: 027-59207879 1972026995 18140587686
Email: sales@3600chem.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: Amadis Chemical Company Limited  
Tel: 571-89925085
Email: sales@amadischem.com
Company Name: Hangzhou Molcore Biopharmatech Co.,Ltd  
Tel: 400-711-5280 86-571-81025280
Email: sales@molcore.com

L-Vinylglycine hydrochloride manufacturers

L-Vinylglycine hydrochloride Basic information
Product Name:L-Vinylglycine hydrochloride
Synonyms:L-Vinylglycine hydrochloride;(S)-vinylglycine hydrochloride;(2S)-2-aminobut-3-enoic acid hydrochloride;L-Vinylglycine HCl;(S)-2-Amino-3-butenoic Acid Hydrochloride;(S)-2-AMinobut-3-enoic acid hydrochloride
CAS:75266-38-5
MF:C4H8ClNO2
MW:137.56482
EINECS:
Product Categories:
Mol File:75266-38-5.mol
L-Vinylglycine hydrochloride Structure
L-Vinylglycine hydrochloride Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
AppearanceWhite to off-white Solid
Optical RotationConsistent with structure
Safety Information
MSDS Information
L-Vinylglycine hydrochloride Usage And Synthesis
Synthesis
(S)-2-(BENZYLOXYCARBONYLAMINO)-3-BUTENOIC ACID METHYL ESTER

75266-40-9

L-Vinylglycine hydrochloride

75266-38-5

General procedure for the synthesis of (S)-2-aminobut-3-enoic acid hydrochloride from (S)-2-(benzyloxycarbonylamino)-3-butenoic acid methyl ester: (S)-2-(benzyloxycarbonylamino)-3-butenoic acid methyl ester (0.905 g, 3.61 mmol) was suspended in 6 M hydrochloric acid solution (20 mL). The reaction mixture was heated to reflux for 2 hours and subsequently cooled to room temperature. Extraction was partitioned with dichloromethane (DCM) and the aqueous phase was again washed with DCM. After combining the organic phases, the aqueous phase was concentrated under vacuum to give a white solid product. Purification by acetone recrystallization resulted in the white crystalline product (S)-2-aminobut-3-enoic acid hydrochloride in a yield of 0.350 g and 71% yield. The structure of the product was confirmed by 1H-NMR (500 MHz, DMSO-d6): δ 8.32 (2H, broad single peak, NH2), 6.02-6.11 (1H, multiple peaks, CH=CH2), 5.50-5.75 (2H, multiple peaks, CH=CH2), 4.68-4.73 (1H, multiple peaks, CHCO2H).

References[1] Tetrahedron, 1985, vol. 41, # 19, p. 4347 - 4358
[2] Journal of Organic Chemistry, 1980, vol. 45, # 24, p. 4817 - 4820
[3] Chemical and Pharmaceutical Bulletin, 1994, vol. 42, # 9, p. 1927 - 1930
[4] Tetrahedron Letters, 1984, vol. 25, # 14, p. 1425 - 1428
[5] Patent: US9434762, 2016, B2. Location in patent: Page/Page column 92
L-Vinylglycine hydrochloride Preparation Products And Raw materials
Raw materials(S)-2-(Benzyloxycarbonylamino)-3-butenoic acid methyl ester-->Water-->Hydrochloric acid-->Dichloromethane
Tag:L-Vinylglycine hydrochloride(75266-38-5) Related Product Information