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Methanamine, N-(benzoyloxy)-N-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92844-59-2

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92844-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92844-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,4 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92844-59:
(7*9)+(6*2)+(5*8)+(4*4)+(3*4)+(2*5)+(1*9)=162
162 % 10 = 2
So 92844-59-2 is a valid CAS Registry Number.

92844-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-nitro-O-benzoylhydroxylamine

1.2 Other means of identification

Product number -
Other names -

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:92844-59-2 SDS

92844-59-2Relevant academic research and scientific papers

Synthesis and Decomposition of the N-Alkyl-N-nitro-O-benzoylhydroxylamines

White, Emil H.,Reefer, John,Erickson, Ronald H.,Dzadzic, Petar M.

, p. 4872 - 4876 (1984)

Nitration of N-alkyl-O-benzoylhydroxylamines yields the correspondng N-nitro derivatives.At modest temperatures these compounds decompose to yield alkyl benzoates, alkenes, benzoic acid, and nitrous oxide.In the case of primary alkylnitrohydroxylamines, nitroalkanes and alkyl nitrates are also formed.The alkyl benzoates are products of ionic reactions since skeletal rearrangements characteristics of carbonium ions occur.The insensivity of the rates of decomposition to solvent polarity suggests that the rate-determining step is a rearrangement rather than direct ionization.

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