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Phenol, 3,5-dimethoxy-4-nitroso- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136491-41-3

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136491-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136491-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,9 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136491-41:
(8*1)+(7*3)+(6*6)+(5*4)+(4*9)+(3*1)+(2*4)+(1*1)=133
133 % 10 = 3
So 136491-41-3 is a valid CAS Registry Number.

136491-41-3SDS

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 3,5-dimethoxy-4-nitrosophenol

1.2 Other means of identification

Product number -
Other names 3,5-Dimethoxy-4-nitroso-phenol

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:136491-41-3 SDS

136491-41-3Relevant academic research and scientific papers

A facile access to substituted 2-nitrosophenols and 2-nitrophenols via regioselective nitrosation of resorcinol monoethers

Maleski,Kluge,Sicker

, p. 2327 - 2335 (2007/10/02)

Solid sodium nitrite in anhydrous propionic acid is an effective system for regioselective nitrosation of the subject compounds. High yields of pure 2-nitroso products are obtained rapidly and efficiently. Attack at the 4-position becomes competitive if water is present in the medium. The 5-alkoxy (but not the 3,5-dialkoxy)-2-nitrosphenols can be easily oxidized with nitric acid to yield the corresponding 2-nitro compounds.

NITROSODEALKYLATION AS A SELECTIVE METHOD FOR THE PRODUCTION OF SUBSTITUTED ORTHO- AND PARA- NITROSOPHENOLS

Shpinel', Ya.I.,Klimova, I.V.,Belyaev, E.Yu.

, p. 1309 - 1312 (2007/10/02)

In the reaction of nitrosylsulfuric acid with sterically hindered phenols and 1,3-dialkoxybenzenes the corresponding o- and p-nitrosophenols are formed.In the series of sterically hindered phenols the reaction is ortho-specific, and this is explained by t

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