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80082-51-5

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  • Carbamicacid, [1-(aminocarbonyl)-2-[(methylsulfonyl)oxy]propyl]-, phenylmethyl ester,[R-(R*,S*)]- (9CI)

    Cas No: 80082-51-5

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80082-51-5 Usage

Chemical Properties

White Solid

Check Digit Verification of cas no

The CAS Registry Mumber 80082-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,8 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80082-51:
(7*8)+(6*0)+(5*0)+(4*8)+(3*2)+(2*5)+(1*1)=105
105 % 10 = 5
So 80082-51-5 is a valid CAS Registry Number.

80082-51-5SDS

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 benzyl (R-(R*,S*))-[1-carbamoyl-2-(mesyloxy)propyl]carbamate

1.2 Other means of identification

Product number -
Other names BENZYL [R-(R*,S*)]-[1-CARBAMOYL-2-(MESYLOXY)PROPYL]CARBAMATE

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:80082-51-5 SDS

80082-51-5Relevant articles and documents

Preparation method of amino-2-methyl-4-oxo-1-azetidinesulfonic acid intermediate

-

Paragraph 0023-0035, (2020/08/25)

The invention discloses a preparation method of an amino-2-methyl-4-oxo-1-azetidinesulfonic acid intermediate, comprising the following steps: S1, adding N-carbobenzoxy-L-threonine amide into a reaction vessel, adding an organic solvent, stirring, mixing, adding 2-methylpyridine and methylsulfonyl chloride, heating, and carrying out a thermal reaction to obtain a reaction solution I; S2, cooling the reaction solution I to below 0 DEG C, then adding chlorosulfonic acid into the cooled reaction solution I, heating, carrying out a thermal reaction to obtain a reaction solution II, and cooling; and S3, adding deionized water into the cooled reaction solution II for a quenching reaction, then adding alkali liquor into the reaction system to adjust the pH, heating, and carrying out a thermal reaction. The method adopts a one-pot method for synthesis, is simple in process operation and short in period, avoids the generation of three wastes, and realizes the production of a green process; thepurity of the obtained amino-2-methyl-4-oxo-1-azetidinesulfonic acid intermediate is as high as 98.5%, the molar yield is as high as 80.9%, the product quality is good, and the method is suitable forindustrial production.

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