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683276-64-4

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683276-64-4 Usage

General Description

R-2-METHYL GLYCIDYL P-NOSYLATE is a chemical compound commonly used as a reagent in organic synthesis. It belongs to the class of glycidyl ethers and is specifically used for the protection of hydroxyl groups in organic molecules. The compound contains a 2-methyl glycidyl group and a p-nosylate group, which are important for its reactivity and selectivity in specific chemical reactions. R-2-METHYL GLYCIDYL P-NOSYLATE is known for its stability and compatibility with a wide range of organic solvents, making it a versatile tool in the field of organic chemistry for the modification and manipulation of complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 683276-64-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,3,2,7 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 683276-64:
(8*6)+(7*8)+(6*3)+(5*2)+(4*7)+(3*6)+(2*6)+(1*4)=194
194 % 10 = 4
So 683276-64-4 is a valid CAS Registry Number.

683276-64-4SDS

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 [(2R)-2-methyloxiran-2-yl]methyl 3-nitrobenzenesulfonate

1.2 Other means of identification

Product number -
Other names 4-Nitro-benzenesulfonic acid (R)-2-methyl-oxiranylmethyl ester

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:683276-64-4 SDS

683276-64-4Relevant articles and documents

Using an asymmetric flow reactor sharples

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Paragraph 0046, (2019/05/21)

PROBLEM TO BE SOLVED: To provide a method for efficiently progressing a Sharpless asymmetric epoxidation even without adding molecular sieves. SOLUTION: The method for producing an optically active epoxyalcohol compound includes mixing an allyl alcohol compound, a titanium tetraalkoxide in a catalytic amount, an optically active tartaric acid ester in a catalytic amount, and an oxidizing agent, in a solvent by using a flow-type reactor (flow reactor). The oxidizing agent is preferably tert-butyl hydroperoxide or cumene hydroperoxide. COPYRIGHT: (C)2013,JPOandINPIT

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