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79612-79-6

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79612-79-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79612-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,1 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79612-79:
(7*7)+(6*9)+(5*6)+(4*1)+(3*2)+(2*7)+(1*9)=166
166 % 10 = 6
So 79612-79-6 is a valid CAS Registry Number.

79612-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-((4-bromophenyl)amino)-3-oxopropanoate

1.2 Other means of identification

Product number -
Other names ethyl ester of p-bromomalonanilic 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:79612-79-6 SDS

79612-79-6Relevant articles and documents

SYNTHESIS AND PROPERTIES OF AMIDES OF 2-SUBSTITUTED 3-ARYL- AND 3-PYRIDYLAMINOACRYLIC ACIDS

Mikhalev, A. I.,Ukhov, S. V.,Konshin, M. E.

, p. 551 - 555 (1994)

The reaction of aryl- or pyridylamines with ethyl orthoformate and malonanilic acid gave amides of 2-(N-arylcarbamoyl)-, 2-cyano-, 2-ethoxycarbonyl-3-aryloaminoacrylic acids and their corresponding 3-pyridyl analogs.IR and PMR spectroscopy indicates that

HCV NS3 PROTEASE INHIBITORS

-

Page/Page column 63; 64, (2013/06/05)

The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.

SIX-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS

-

Page/Page column 101, (2008/06/13)

The present invention provides compounds of Formula (I), or a stereoisomer, tautomer, pharmaceutically acceptable salt or solvate form thereof, wherein the variables A, B, R3 and R11 are as defined herein. The compounds of Formula (I) are useful as selective inhibitors of serine protease enzymes of the coagulation cascade and/or contact activation system; for example thrombin, factor Xa, factor XIa, factor IXa, factor VIIa and/or plasma kallikrein. In particular, it relates to compounds that are selective factor XIa inhibitors or dual inhibitors of fXIa and plasma kallikrein. This invention also relates to pharmaceutical compositions comprising these compounds and methods of treating thromboembolic and/or inflammatory disorders using the same.

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