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6192-01-4

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6192-01-4 Usage

Synthesis Reference(s)

Synthesis, p. 1016, 1986 DOI: 10.1055/s-1986-31854

Check Digit Verification of cas no

The CAS Registry Mumber 6192-01-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6192-01:
(6*6)+(5*1)+(4*9)+(3*2)+(2*0)+(1*1)=84
84 % 10 = 4
So 6192-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O3/c1-2-8-4-3-5(6)7/h3-4H,2H2,1H3,(H,6,7);

6192-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Ethoxyacrylic Acid

1.2 Other means of identification

Product number -
Other names 3-ETHOXYACRYLIC ACID

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:6192-01-4 SDS

6192-01-4Relevant articles and documents

UDP GLYCOSYLTRANSFERASE INHIBITORS AND METHODS OF USE

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Paragraph 1325; 1326, (2020/04/24)

Described herein is a compound of Formula (I), and pharmaceutically acceptable salts thereof. Also described herein are compositions and the use of such compositions in methods of treating a variety of diseases and conditions, in particular Krabbe's Disease (KD) and Metachromatic leukodystrophy (MLD).

INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE

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Page/Page column 333, (2018/06/30)

Compounds of formula (I') and methods of their use and preparation, as well as compositions comprising compounds of formula (I').

Enantioselective Synthesis of N?H-Free 1,5-Benzothiazepines

Wang, Guojin,Tang, Yu,Zhang, Yu,Liu, Xiaohua,Lin, Lili,Feng, Xiaoming

supporting information, p. 554 - 557 (2017/01/18)

An enantioselective sulfa-Michael-cyclization reaction was developed for the synthesis of 1,5-benzothiazepines with versatile pharmacological activities. The reaction between 2-aminothiophenol and α,β-unsaturated pyrazoleamides gave direct access to N?H-free 1,5-benzothiazepines in the presence of a chiral N,N′-dioxide/Yb(OTf)3complex. Excellent enantioselectivities (up to 96 % ee) and high yields (up to 99 %) were obtained for a broad range of substrates under mild reaction conditions. This method provided a facile approach to the antidepressant drug (R)-(?)-Thiazesim.

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