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128677-61-2

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128677-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128677-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,6,7 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128677-61:
(8*1)+(7*2)+(6*8)+(5*6)+(4*7)+(3*7)+(2*6)+(1*1)=162
162 % 10 = 2
So 128677-61-2 is a valid CAS Registry Number.

128677-61-2SDS

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 (R)-4-BENZYL-2-OXAZOLIDINONE LITHIUM SALT

1.2 Other means of identification

Product number -
Other names lithium salt of (S)-4-benzyl-2-oxazolidinone

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:128677-61-2 SDS

128677-61-2Relevant articles and documents

3,5-DIAMINO-6-CHLORO-N-(N-(4-PHENYLBUTYL)CARBAMIMIDOYL) PYRAZINE-2- CARBOXAMIDE COMPOUNDS

-

Page/Page column 79; 80; 81; 91; 94, (2014/07/08)

The present invention relates compounds of the formula: or pharmaceutically acceptable salts thereof, useful as sodium channel blockers, as well as compositions containing the same, processes for the preparation of the same, and therapeutic methods of use therefore in promoting hydration of mucosal surfaces and the treatment of diseases including cystic fibrosis, chronic obstructive pulmonary disease, asthma, bronchiectasis, acute and chronic bronchitis, emphysema, and pneumonia.

Asymmetric synthesis of (E)-dehydroapratoxin A

Ma, Jing-Yi,Huang, Wei,Wei, Bang-Guo

scheme or table, p. 4598 - 4601 (2011/09/30)

An asymmetric approach to key intermediate 17 starting from lactone 7 is described, in which Evan's alkylation and CBS-catalyzed reduction are used for construction of the chiral centers, respectively. Thus, the synthesis of (E)-dehydroapratoxin A 6 could

N-FORMYL HYDROXYLAMINE COMPOUNDS

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Page/Page column 18-19, (2008/06/13)

Novel N-formyl hydroxylamine compounds and their derivatives are disclosed. These N-formyl hydroxylamine compounds inhibit peptidyl deformylase (PDF), an enzyme present in prokaryotes. The compounds are useful as antimicrobials and antibiotics. The compou

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