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4-methyl-3-nitrophenyl methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16296-53-0

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16296-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16296-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,9 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16296-53:
(7*1)+(6*6)+(5*2)+(4*9)+(3*6)+(2*5)+(1*3)=120
120 % 10 = 0
So 16296-53-0 is a valid CAS Registry Number.

16296-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-3-nitrophenyl methanesulfonate

1.2 Other means of identification

Product number -
Other names 2-nitro-4-mesyloxy toluene

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:16296-53-0 SDS

16296-53-0Upstream product

16296-53-0Relevant academic research and scientific papers

Synthesis of the Indolocarbazole Natural Products Staurosporinone and Arcyriaflavin B

Hughes, Ian,Nolan, William P.,Raphael, Ralph A.

, p. 2475 - 2480 (2007/10/02)

Flexible synthetic routes involving double nitrene insertions are described leading to the indolocarbazole systems present in a growing group of natural products.The methods are exemplified by the total synthesis of two members of this group stauro

2-Amino-4-hydroxy-5-chloro toluene and the hydrochloride thereof

-

, (2008/06/13)

2-Amino-4-hydroxy-5-chloro toluene and the hydrochloride thereof are couplers usefully employed in the production of a hair dye by reaction with an aromatic paradiamine.

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