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dimethyl [(chloroacetyl)amino]propanedioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74084-50-7

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74084-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74084-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,8 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74084-50:
(7*7)+(6*4)+(5*0)+(4*8)+(3*4)+(2*5)+(1*0)=127
127 % 10 = 7
So 74084-50-7 is a valid CAS Registry Number.

74084-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-[(2-chloroacetyl)amino]propanedioate

1.2 Other means of identification

Product number -
Other names 2-(2-chloro-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:74084-50-7 SDS

74084-50-7Downstream Products

74084-50-7Relevant academic research and scientific papers

COMPLEX-FORMING COMPOUNDS

-

Page/Page column 26, (2013/07/19)

Present invention refers to complex-forming compounds of the general formula and the use and preparation thereof.

New insertion reactions of some carbenoids into amide- and sulfonamide-NH bonds

Mloston,Celeda,Swiatek,Kaegi,Heimgartner

, p. 1907 - 1914 (2007/10/03)

In the presence of catalytic amounts of Rh2(OAc)4 in toluene, dimethyl diazomalonate (1) decomposed with evolution of N2 to form a carbenoid of type 8 which reacted with carboxamides 2 and toluenesulfonamide (4) to give 2-(acylamino)- and 2-(sulfonylamino)malonates 3 and 5, respectively. In an analogous reaction, α-diazo ketone 6 and 4 yielded N-(2-oxo-1,2-diphenylethyl)toluenesulfonamide (7).

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