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2-Methoxy-1,3-dimethyl-1,3,2-diazaphospholidine is a heterocyclic compound characterized by a phosphorus atom bonded to two nitrogen atoms, forming a three-membered ring. This molecule features a methoxy group (-OCH3) at the 2-position and two methyl groups (-CH3) at the 1 and 3 positions. The presence of the methoxy group imparts electron-donating properties, while the methyl groups provide steric hindrance. 2-methoxy-1,3-dimethyl-1,3,2-diazaphospholidine is of interest in organic chemistry and may have potential applications in the synthesis of various phosphorus-containing compounds, such as phosphazenes and other organophosphorus derivatives. Its unique structure and reactivity make it a valuable building block for the development of new materials and pharmaceuticals.

7137-86-2

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7137-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7137-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7137-86:
(6*7)+(5*1)+(4*3)+(3*7)+(2*8)+(1*6)=102
102 % 10 = 2
So 7137-86-2 is a valid CAS Registry Number.

7137-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-1,3-dimethyl-1,3,2-diazaphospholidine

1.2 Other means of identification

Product number -
Other names Methoxy-2 dimethyl-1,3 diazaphospholan-1,3,2

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

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More Details:7137-86-2 SDS

7137-86-2Relevant academic research and scientific papers

EFFICIENT OLEFINATION WITH α-ALKYL CYCLIC PHOSPHONAMIDES

Hanessian, Stephen,Bennani, Youssef L.,Leblanc, Yves

, p. 1411 - 1424 (2007/10/02)

A variety of acyclic and cyclic aldehydes and ketones can be converted into the corresponding alkylidene, benzylidene and methoxycarbonyl alkylidene derivatives by treatment with 1,3,2-diazaphospholidine-2-alkyl-1,3-dimethyl 2-oxides (α-alkyl cyclic phosphonamides) under mild conditions.This olefination method is particularly useful in the case of enolizable carbonyl compounds.

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