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124044-11-7

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124044-11-7 Usage

General Description

Methyl 2-(N-benzoylaminomethyl)-3-oxobutyrate is a chemical compound with the molecular formula C14H15NO4. It is an ester with a benzoylaminomethyl group attached to the second carbon of the butyrate chain. Methyl 2-(N-benzoylaminomethyl)-3-oxobutyrate is commonly used in the synthesis of pharmaceuticals and organic compounds due to its versatile reactivity and functional groups. It has a wide range of applications in the pharmaceutical and chemical industries, including as an intermediate for the production of various drugs and as a reagent in organic synthesis. Methyl 2-(N-benzoylaminomethyl)-3-oxobutyrate is a valuable and important compound with multiple industrial and commercial uses.

Check Digit Verification of cas no

The CAS Registry Mumber 124044-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,4 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124044-11:
(8*1)+(7*2)+(6*4)+(5*0)+(4*4)+(3*4)+(2*1)+(1*1)=77
77 % 10 = 7
So 124044-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO4/c1-9(15)11(13(17)18-2)8-14-12(16)10-6-4-3-5-7-10/h3-7,11H,8H2,1-2H3,(H,14,16)

124044-11-7SDS

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 Methyl 2-[(benzoylamino)methyl]-3-oxobutanoate

1.2 Other means of identification

Product number -
Other names -

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:124044-11-7 SDS

124044-11-7Relevant articles and documents

Preparation method of 4AA

-

, (2021/07/28)

The invention discloses a preparation method of 4AA. The preparation method comprises the following steps: S1, preparing a first intermediate from benzamide and a formaldehyde aqueous solution; S2, preparing a second intermediate from the first intermediate, thionyl chloride, toluene and n-heptane; S3, preparing a third intermediate from the second intermediate, methyl acetoacetate, sodium methoxide, toluene, diluted hydrochloric acid and isopropanol; S4, preparing a fourth intermediate from the third intermediate, reductase, ethyl acetate, saturated sodium bicarbonate and saturated salt water; S5, preparing a fifth intermediate from the fourth intermediate, imidazole, TBSCL and methylbenzene; S6, preparing a sixth intermediate from the fifth intermediate, ethanolamine, methanol and n-heptane; S7, preparing a seventh intermediate by using the sixth intermediate, a Grignard reagent and n-heptane; and S8, preparing 4AA from the seventh intermediate, ruthenium trichloride, potassium acetate, ethyl acetate, acetic acid and a peracetic acid solution.

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