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149498-94-2

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  • ETHYL 3-AMINO-3-(1,3-BENZODIOXOL-5-YL)PROPANOATE HYDROCHLORIDE

    Cas No: 149498-94-2

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149498-94-2 Usage

Uses

3-Amino-3-benzo[1,3]dioxol-5-yl-propionic acid ethyl ester, HCl

Check Digit Verification of cas no

The CAS Registry Mumber 149498-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,4,9 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149498-94:
(8*1)+(7*4)+(6*9)+(5*4)+(4*9)+(3*8)+(2*9)+(1*4)=192
192 % 10 = 2
So 149498-94-2 is a valid CAS Registry Number.

149498-94-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-3-benzo[1,3]dioxol-5-yl-propionic acid ethyl ester hydrochloride

1.2 Other means of identification

Product number -
Other names 2,4-Dibrom-buttersaeure-aethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:149498-94-2 SDS

149498-94-2Relevant articles and documents

An efficient new enzymatic method for the preparation of β-aryl-β-amino acid enantiomers

Tasnadi, Gabor,Forro, Eniko,Fueloep, Ferenc

, p. 2072 - 2077 (2008/12/22)

An efficient synthesis of β-aryl-β-amino acid enantiomers has been developed via the lipase-catalysed enantioselective hydrolysis of the corresponding racemic ethyl esters in an organic solvent. High enantioselectivities (E >100) were observed when the lipase PS-catalysed reactions were performed with H2O (0.5 equiv) in diisopropyl ether at 45 °C. The products could be easily separated and were obtained in good yields of ≥40%.

Potent in vitro and in vivo inhibitors of platelet aggregation based upon the Arg-Gly-Asp sequence of fibrinogen. (Aminobenzamidino)succinyl (ABAS) series of orally active fibrinogen receptor antagonists

Zablocki,Rico,Garland,Rogers,Williams,Schretzman,Rao,Bovy,Tjoeng,Lindmark,Toth,Zupec,McMackins,Adams,Miyano,Markos,Milton,Paulson,Herin,et al.

, p. 2378 - 2394 (2007/10/02)

Our initial orally active fibrinogen receptor antagonist benzamidinopentanoyl (BAP) series which was discovered through truncation of our iv antiplatelet agent (SC-52012) demonstrated modest oral activity in canine studies (ethyl [5-(4-amidinophenyl)penta

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