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51575-86-1

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51575-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51575-86-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,7 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51575-86:
(7*5)+(6*1)+(5*5)+(4*7)+(3*5)+(2*8)+(1*6)=131
131 % 10 = 1
So 51575-86-1 is a valid CAS Registry Number.

51575-86-1SDS

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 meso dimethyl α,β-dibromosuccinate

1.2 Other means of identification

Product number -
Other names dimethyl 2,3-dibromobutane-1,4-dicarboxylate

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:51575-86-1 SDS

51575-86-1Relevant articles and documents

Preparation method of chiral ligand(3S, 4S)-2, 5-dioxotetrahydrofuran-3, 4-bis(benzyl carbamate)

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Paragraph 0042-0044, (2020/06/17)

The invention relates to the field of chiral transition metal catalysts, and relates to a preparation method of a chiral ligand(3S, 4S)-2, 5-dioxotetrahydrofuran-3, 4-bis(benzyl carbamate). The methodcomprises the following steps: taking internal compensation 1, 3-dibromosuccinic acid as a raw material; carrying out esterification reaction under the catalysis of acid to generate diester (I); carrying out nucleophilic substitution reaction on the compound (I) and amine to obtain a compound (II); carrying out a removal reaction on the compound (II) under the action of trifluoroacetic acid to obtain amino diester (III); carrying out acylation reaction on the compound (III) and acyl chloride to obtain amide (IV); and hydrolyzing the ester group of the compound (IV) into acid (V) under an alkaline condition, and finally performing intramolecular dehydration on the compound (V) to obtain the chiral transition metal catalyst intermediate. The invention provides a simple and convenient industrial production route for the chiral transition metal catalyst intermediate, the reaction operation is simple, the use of an expensive palladium reagent is avoided, and the cost is lower.

Thiophene Analogues of the Alkaloids. Part 6. Synthesis of Thiophene Analogues of Some 1-Benzylisoquinolines.

Huddleston, Patrick R.,Barker, John M.,Stickland, Barbara,Wood, Michael L.,Guindi, Laila H. M.

, p. 1871 - 1890 (2007/10/02)

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