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67654-57-3

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67654-57-3 Usage

General Description

Methyl (R)-3-acetamido-3-phenylpropanoate is a chemical compound with the molecular formula C12H15NO3. It is a chiral compound, meaning it has a non-superimposable mirror image, and the (R)- designation indicates its stereochemistry. Methyl (R)-3-acetamido-3-phenylpropanoate is commonly used in the pharmaceutical industry for the synthesis of various drugs and active pharmaceutical ingredients. It is also used as a key intermediate in the production of enantiomerically pure compounds, which are important for the development of many pharmaceutical and agrochemical products. Methyl (R)-3-acetamido-3-phenylpropanoate plays a crucial role in the preparation of a wide range of biologically active molecules, making it a valuable compound in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 67654-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,5 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67654-57:
(7*6)+(6*7)+(5*6)+(4*5)+(3*4)+(2*5)+(1*7)=163
163 % 10 = 3
So 67654-57-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO3/c1-9(14)13-11(8-12(15)16-2)10-6-4-3-5-7-10/h3-7,11H,8H2,1-2H3,(H,13,14)/t11-/m1/s1

67654-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (R)-3-acetamido-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names (R)-methyl-3-acetamido-3-phenylpropanoate

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:67654-57-3 SDS

67654-57-3Relevant articles and documents

OPTICALLY ACTIVE BISPHOSPHINO METHANE AND PRODUCTION METHOD THEREFOR, AND TRANSITION METAL COMPLEX AND ASYMMETRIC CATALYST

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Paragraph 0071-0073, (2021/02/10)

PROBLEM TO BE SOLVED: To provide a novel optically active bisphosphine methane that is useful as a ligand for an asymmetric catalyst, has excellent oxidation resistance in the air, and is easy to handle, and to provide a transition metal complex using, as

Chiral ferrocene-indole diphosphine ligand as well as preparation method and application thereof

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Paragraph 0067-0068, (2021/05/22)

The invention relates to a chiral ferrocene-indole diphosphine ligand as well as a preparation method and application thereof. The specific preparation method comprises the following steps: dissolving an indole compound and a chiral ferrocene phosphine ac

Nickel-catalyzed enantioselective umpolung hydrogenation for stereoselective synthesis of β-amido esters

Zhou, Jianrong Steve,Guo, Siyu,Zhao, Xiaohu,Chi, Yonggui Robin

supporting information, p. 11501 - 11504 (2021/11/16)

Nickel complexes ligated by strongly donating diphosphines catalyze enantioselective hydrogenation for the preparation of acyclic and cyclic β-amido esters. A combination of acetic acid and indium powder provides protons and electrons to form nickel hydrido complexes under umpolung hydrogenation conditions.

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