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88470-26-2

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88470-26-2 Usage

General Description

Hydroxylamine, N-methoxy-O-methyl- is a chemical compound with the molecular formula CH5NO2. It is a derivative of hydroxylamine, a reagent commonly used in organic synthesis and pharmaceutical research. N-methoxy-O-methyl-hydroxylamine is used as a reagent in the synthesis of organic compounds, particularly in the formation of oximes and various heterocyclic compounds. It has also been studied for its potential medical applications, such as its anti-inflammatory and anti-cancer properties. However, it is important to handle this chemical with caution, as it can be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 88470-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,7 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88470-26:
(7*8)+(6*8)+(5*4)+(4*7)+(3*0)+(2*2)+(1*6)=162
162 % 10 = 2
So 88470-26-2 is a valid CAS Registry Number.

88470-26-2SDS

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 (methoxyamino)oxymethane

1.2 Other means of identification

Product number -
Other names Dimethoxyamine

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:88470-26-2 SDS

88470-26-2Relevant articles and documents

N,N-DIALKOXY-N'-ALKYLUREAS

Rudchenko, V. F.,Ignatov, S. M.,Kostyanovskii, R. G.

, p. 1920 - 1921 (2007/10/02)

The chlorination of N-alkoxy-N'-alkylureas (1) by the action of t-BuOCl proceeds regiospecifically to give stable N-chloro-N-alkoxy-N'-alkylureas (2).The alcoholysis of 2 leads to N,N-dialkoxy-N'-alkylureas (3).The alkaline hydrolysis of 3 is a new, convenient method for the preparation of dialkoxyamines.Keywords: N-alkoxy-N'-alkylureas, N-chloro-N-alkoxy-N'-aklylureas, N,N-dialkoxy-N'-alkylureas, dialkoxyamines.

N,N-DIALKOXYUREAS AND NH-DIALKOXYAMINES

Rudchenko, V. F.,Shevchenko, V. I.,Ignatov, S. M.,Kostyanovskii, R. G.

, p. 2174 (2007/10/02)

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