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60190-78-5

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60190-78-5 Usage

General Description

Acetic acid, diazo(dimethoxyphosphinyl)-, methyl ester is a chemical compound with the molecular formula C4H9O4NP. It is commonly used as a reagent in organic synthesis, particularly in the preparation of phosphorus-based compounds. Acetic acid, diazo(dimethoxyphosphinyl)-, methyl ester is a methyl ester of diazo(dimethoxyphosphinyl)acetic acid, and it is known for its diazo group, which contains two methoxyphosphinyl groups. It is a colorless to pale yellow liquid with a pungent odor, and it is considered to be highly flammable and potentially hazardous if not handled with care. Acetic acid, diazo(dimethoxyphosphinyl)-, methyl ester is primarily used in research and industrial applications, and it is important to handle it with caution due to its potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 60190-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,9 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60190-78:
(7*6)+(6*0)+(5*1)+(4*9)+(3*0)+(2*7)+(1*8)=105
105 % 10 = 5
So 60190-78-5 is a valid CAS Registry Number.

60190-78-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-diazonio-2-dimethoxyphosphoryl-1-methoxyethenolate

1.2 Other means of identification

Product number -
Other names (MeO)2P(O)C(N2)COMe

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:60190-78-5 SDS

60190-78-5Relevant articles and documents

Total synthesis and structural confirmation of (±)-cuevaene A

Craven, Philip G.E.,Taylor, Richard J.K.

, p. 5422 - 5425 (2012)

The total synthesis and structural reassignment of cuevaene A have been completed. The key synthetic steps in the total synthesis included a base-promoted double conjugate addition and further elaboration to generate the tricyclic core structure, followed by construction of the trienoic acid side chain. Detailed comparison of proton and carbon NMR data with published values enabled the connectivity of the natural product, which had been debated in earlier publications, to be confirmed.

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