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3-(2-CHLORO-3,4-DIMETHOXYPHENYL)ACRYLAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

175135-98-5

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175135-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175135-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 175135-98:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*5)+(2*9)+(1*8)=145
145 % 10 = 5
So 175135-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H12ClNO3/c1-15-8-5-3-7(4-6-9(13)14)10(12)11(8)16-2/h3-6H,1-2H3,(H2,13,14)/b6-4+

175135-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-chloro-3,4-dimethoxyphenyl)prop-2-enamide

1.2 Other means of identification

Product number -
Other names 2-Propenamide,3-(2-chloro-3,4-dimethoxyphenyl)

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:175135-98-5 SDS

175135-98-5Downstream Products

175135-98-5Relevant academic research and scientific papers

Sequential rhodium/palladium catalysis: Enantioselective formation of dihydroquinolinones in the presence of achiral and chiral ligands

Zhang, Lei,Qureshi, Zafar,Sonaglia, Lorenzo,Lautens, Mark

supporting information, p. 13850 - 13853 (2015/01/16)

Compatible combinations of achiral and chiral ligands can be used in rhodium/palladium catalysis to achieve highly enantioselective domino reactions. The difference in rates of catalysis and minimal effects of ligand interference confer control in the dom

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