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126063-08-9

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126063-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126063-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,6 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 126063-08:
(8*1)+(7*2)+(6*6)+(5*0)+(4*6)+(3*3)+(2*0)+(1*8)=99
99 % 10 = 9
So 126063-08-9 is a valid CAS Registry Number.

126063-08-9SDS

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 2,2,2-trifluoro-N-(4-iodophenyl)acetamide

1.2 Other means of identification

Product number -
Other names N-(Trifluoroacetyl)-4-iodoaniline

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:126063-08-9 SDS

126063-08-9Relevant articles and documents

A Simple and Economical Synthetic Route to p-Ethynylaniline and Ethynyl-Terminated Substrates

Melissaris, Anastasios P.,Litt, Morton H.

, p. 5818 - 5821 (1994)

-

Switching reaction pathways of trifluoromethylated thiobenzanilides by choice of different oxidative systems

Zhu, Jiangtao,Xie, Haibo,Li, Shan,Chen, Zixian,Wu, Yongming

, p. 306 - 309 (2011/06/20)

Trifluoromethylated thiobenzanilides are efficiently converted to 2-trifluoromethylbenzothiazoles via intramolecular oxidative cyclization under CAN/NaHCO3 oxidation, while the dimerized products with "-S-S-" bond linkage are obtained when PIDA

Sulfonylaminovalerolactams and derivatives thereof as factor Xa inhibitors

-

Page/Page column 48, (2008/06/13)

The present application describes sulfonylaminovalerolactams and derivatives thereof of Formula I: or pharmaceutically acceptable salt forms thereof, wherein ring G is a mono- or bicyclic carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.

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