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27491-70-9

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27491-70-9 Usage

Chemical Properties

Yellow Oil

Uses

Different sources of media describe the Uses of 27491-70-9 differently. You can refer to the following data:
1. Reagent for one-carbon homologation of aldehydes and ketones to alkynes.
2. Seyferth-Gilbert Reagent

Check Digit Verification of cas no

The CAS Registry Mumber 27491-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,9 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27491-70:
(7*2)+(6*7)+(5*4)+(4*9)+(3*1)+(2*7)+(1*0)=129
129 % 10 = 9
So 27491-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H8N2O3P/c1-7-9(6,8-2)3-5-4/h3-4H,1-2H3/q+1

27491-70-9SDS

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 diazo(dimethoxyphosphoryl)methane

1.2 Other means of identification

Product number -
Other names diazomethyl-phosphonic acid dimethyl ester

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:27491-70-9 SDS

27491-70-9Relevant articles and documents

Application of FSO2N3 in preparation of diazo reagent

-

Paragraph 0111-0119, (2021/06/06)

The invention discloses application of FSO2N3 in preparation of a diazo reagent. The application comprises the following step: in the presence of alkali, FSO2N3 and acetone dimethyl phosphate as shown in a formula 2 are subjected to a reaction as shown in the specification, and a Bestmann-Ohira and/or Seyferth-Gilbert reagent is obtained. According to the application, the Seyferth-Gilbert reagent and/or the Bestmann-Ohira reagent can be obtained at a high yield in half an hour, the two mixed reagents generated in the reaction do not need to be separated, and the one-pot method is directly applied to the synthesis of the terminal alkyne compound. And/or like.

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