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66947-88-4

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66947-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66947-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,4 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66947-88:
(7*6)+(6*6)+(5*9)+(4*4)+(3*7)+(2*8)+(1*8)=184
184 % 10 = 4
So 66947-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClINO/c9-5-8(12)11-7-4-2-1-3-6(7)10/h1-4H,5H2,(H,11,12)

66947-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-N-(2-iodophenyl)acetamide

1.2 Other means of identification

Product number -
Other names chloro-acetic acid-(2-iodo-anilide)

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:66947-88-4 SDS

66947-88-4Downstream Products

66947-88-4Relevant articles and documents

Cyclative Cascades of Allenamides Derived from Amino Acids: Synthesis of Annulated Indoxyl Derivatives

Petkovic, Milos,Nasufovic, Veselin,Djukanovic, Dimitrije,Vujosevic, Zorana Tokic,Jadranin, Milka,Matovic, Radomir,Savic, Vladimir

, p. 1279 - 1282 (2016)

Allenamides derived from amino acids participate in the cascade transformations catalyzed by Pd0 allowing consecutive formation of two five-membered rings. The developed methodology provides an access to annulated indoles which can be transform

Tri-substituted triazoles as potent non-nucleoside inhibitors of the HIV-1 reverse transcriptase

De La Rosa, Martha,Kim, Hong Woo,Gunic, Esmir,Jenket, Cheryl,Boyle, Uyen,Koh, Yung-hyo,Korboukh, Ilia,Allan, Matthew,Zhang, Weijian,Chen, Huanming,Xu, Wen,Nilar, Shahul,Yao, Nanhua,Hamatake, Robert,Lang, Stanley A.,Hong, Zhi,Zhang, Zhijun,Girardet, Jean-Luc

, p. 4444 - 4449 (2007/10/03)

A new series of 1,2,4-triazoles was synthesized and tested against several NNRTI-resistant HIV-1 isolates. Several of these compounds exhibited potent antiviral activities against efavirenz- and nevirapine-resistant viruses, containing K103N and/or Y181C mutations or Y188L mutation. Triazoles were first synthesized from commercially available substituted phenylthiosemicarbazides, then from isothiocyanates, and later by condensing the desired substituted anilines with thiosemicarbazones.

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