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65102-57-0

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65102-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65102-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,0 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65102-57:
(7*6)+(6*5)+(5*1)+(4*0)+(3*2)+(2*5)+(1*7)=100
100 % 10 = 0
So 65102-57-0 is a valid CAS Registry Number.

65102-57-0SDS

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-benzoyloxy-2-(benzoyloxymethyl)-2-nitropropyl] benzoate

1.2 Other means of identification

Product number -
Other names 1,3-Bis-benzoyloxy-2-benzoyloxymethyl-2-nitro-propan

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:65102-57-0 SDS

65102-57-0Downstream Products

65102-57-0Relevant articles and documents

Preparation method of 3-oxetanecarboxylic acid

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Paragraph 0066; 0068-0070; 0092; 0114, (2018/09/12)

The invention provides a preparation method of 3-oxetanecarboxylic acid. According to the preparation method, 2-hydroxymethyl-2-nitro-1,3-propylene glycol is taken as a raw material, hydroxyl in 2-hydroxymethyl-2-nitro-1,3-propylene glycol is subjected to a group protection reaction, nitryl in 2-hydroxymethyl-2-nitro-1,3-propylene glycol is subjected to a reductive elimination reaction and hydrolysis reaction, and 2-hydroxymethyl-1,3-propylene glycol is obtained; 2-hydroxymethyl-1,3-propylene glycol is continuously subjected to a cyclization reaction and an oxidation reaction, and 3-oxetanecarboxylic acid is obtained. The provided preparation method can be completed only through five-step reactions; compared with existing preparation methods through ten-step reactions, the preparation method has the advantages that the reaction steps are greatly reduced, the reaction routes are greatly shortened, the overall yield is increased, and the final yield can be up to 50% or above on the basisof the raw material, namely, 2-hydroxymethyl-2-nitro-1,3-propylene glycol; the related reactions are simple, and the method is easy to operate and favorable for industrial production.

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