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651738-74-8

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651738-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651738-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,7,3 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 651738-74:
(8*6)+(7*5)+(6*1)+(5*7)+(4*3)+(3*8)+(2*7)+(1*4)=178
178 % 10 = 8
So 651738-74-8 is a valid CAS Registry Number.

651738-74-8SDS

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-Cyclohexyl-N-hydroxypropanamide

1.2 Other means of identification

Product number -
Other names Cyclohexanepropanamide,N-hydroxy

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:651738-74-8 SDS

651738-74-8Downstream Products

651738-74-8Relevant articles and documents

Synthesis of Lactams via Ir-Catalyzed C-H Amidation Involving Ir-Nitrene Intermediates

Li, Xiaoxun,Liu, Jitian,Tang, Weiping,Wang, Shuojin,Ye, Wenjing,Zheng, Junrong

, (2020/03/19)

x-membered lactams were synthesized via either an amidation of sp3 C-H bonds or an electrophilic substitution of arenes via Ir-nitrene intermediates. With the employment of a readily available iridium catalyst in dichloromethane or hexafluoro-2-propanol, a wide range of lactams were synthesized in good to excellent yields with high selectivity.

A two-step tandem reaction to prepare hydroxamic acids directly from alcohols

Dettori, Giovanna,Gaspa, Silvia,Porcheddu, Andrea,De Luca, Lidia

supporting information, p. 4582 - 4585 (2014/06/24)

The first synthesis of hydroxamic acids from alcohols has been developed. Both benzylic and aliphatic alcohols can be tolerated and applied in this reaction. The methodology is economical, environmentally benign and high yielding. This journal is

NOVEL COMPOUNDS AS HISTONE DEACETYLASE INHIBITORS

-

Page 16, (2008/06/13)

The present invention is directed to compounds of the general formula (I) or pharmaceutical acceptable salts or physiologically functional derivatives thereof wherein: n is a non-aromatic ring system containing two to seven carbon atoms, wherein the ring

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