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60187-67-9

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60187-67-9 Usage

General Description

Dimethyl acetamidomalonate is an organic compound with the chemical formula C7H11NO5. It is derived from malonic acid through an amidation reaction with dimethyl acetamide. Dimethyl acetamidomalonate is used as a building block in organic synthesis and is a versatile intermediate in the pharmaceutical industry. It is also used as a reagent in the synthesis of biologically active molecules, such as antitumor and antiviral agents. Dimethyl acetamidomalonate has potential applications in the development of new drugs and pharmaceutical products due to its ability to introduce various functional groups and stereochemistry into complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 60187-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,8 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60187-67:
(7*6)+(6*0)+(5*1)+(4*8)+(3*7)+(2*6)+(1*7)=119
119 % 10 = 9
So 60187-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO5/c1-4(9)8-5(6(10)12-2)7(11)13-3/h5H,1-3H3,(H,8,9)

60187-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-acetamidopropanedioate

1.2 Other means of identification

Product number -
Other names acetylamino-malonic 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:60187-67-9 SDS

60187-67-9Relevant articles and documents

Reaction of Dicarbomethoxycarbene with Acetaldehyde and Simple Ketones

L'Esperance, Robert P.,Ford, Thomas M.,Jones, Maitland

, p. 209 - 213 (2007/10/02)

Singlet dicarbomethoxycarbene reacts with acetaldehyde to give dioxolane 8, the ultimate product of formation of ylide 10 and subsequent addition of a second molecule of aldehyde.Photosensitized generation of the carbene gives increased hydrogen abstraction and decreased products derived from the ylide.Replacement of the aldehyde with a ketone changes the course of the reaction and dioxolanes (11, 20, and 26) become the major products.Suggestions are made for the mechanisms of the singlet and triplet reactions and for the peculiar behavior of acetone in which generation of singlet and triplet carbene gives the same product slate.

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