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59511-72-7

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59511-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59511-72-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,1 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59511-72:
(7*5)+(6*9)+(5*5)+(4*1)+(3*1)+(2*7)+(1*2)=137
137 % 10 = 7
So 59511-72-7 is a valid CAS Registry Number.

59511-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-(2-oxoazetidin-3-yl)carbamate

1.2 Other means of identification

Product number -
Other names 3-benzyloxycarbonylamino-2-azetidinone

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:59511-72-7 SDS

59511-72-7Relevant articles and documents

Selective sodium channel regulator as well as preparation and application thereof

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Paragraph 0697-0698; 0705-0706, (2021/02/10)

The invention provides a compound serving as a selective sodium channel regulator and a synthesis and use method, and particularly provides a compound shown as a formula (I), a preparation method of the compound and application of the compound serving as the selective sodium channel regulator. The compounds exhibit excellent activity as a regulator of sodium channels.

2-OXO-1-AZETIDINESULFONIC ACID SALTS

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, (2008/06/13)

Antibacterial activity is exhibited by beta-lactams having a sulfonic acid salt substituent in the 1-position and an amino or acylamino substituent in the 3-position.

N-Acyloxy monocyclic β-lactams

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, (2008/06/13)

Process for N-acyloxy or sulfooxy 2-azetidinones comprising O-acylation of a β-hydroxy or β-halo hydroxamic acid, and cyclizing the O-acylhydroxamate with TPP-CCl4 -TEA or with TPP-dialkylazodicarboxylate to the N-acyloxy-2-azetidinone. Solvoly

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