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67654-58-4

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67654-58-4 Usage

General Description

Methyl (S)-3-acetamido-3-phenylpropanoate is a chemical compound that belongs to the class of esters. It is composed of a methyl group, an acetamido group, and a phenylpropanoate group. Methyl (S)-3-acetamido-3-phenylpropanoate is a chiral molecule with a specific spatial arrangement of atoms, denoted by the (S) designation in its name. It is commonly used in organic synthesis and pharmaceutical research as a building block for the preparation of various pharmacologically active compounds. Its unique structure and properties make it a valuable intermediate in the synthesis of bioactive molecules and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 67654-58-4 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 67654-58:
(7*6)+(6*7)+(5*6)+(4*5)+(3*4)+(2*5)+(1*8)=164
164 % 10 = 4
So 67654-58-4 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-/m0/s1

67654-58-4SDS

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 (3S)-3-acetamido-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names methyl (S)-3-acetylamino-3-phenylpropionate

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:67654-58-4 SDS

67654-58-4Downstream Products

67654-58-4Relevant articles and documents

2,3-BISPHOSPHINOPYRAZINE DERIVATIVE, METHOD FOR PRODUCING SAME, TRANSITION METAL COMPLEX, ASYMMETRIC CATALYST, AND METHOD FOR PRODUCING ORGANIC BORON COMPOUND

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Paragraph 0262-0264, (2021/02/19)

Provided is a 2,3-bisphosphinopyrazine derivative represented by the following general formula (1), wherein R1, R2, R3, and R4 represent an optionally substituted straight-chain or branched alkyl group having 1 to 10 carbon atoms, an optionally substituted cycloalkyl group, an optionally substituted adamantyl group, or an optionally substituted phenyl group, R5 represents an optionally substituted alkyl group having 1 to 10 carbon atoms or an optionally substituted phenyl group, each R5 may be the same group or a different group, R6 represents a monovalent substituent, n denotes an integer of 0 to

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

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Paragraph 0046-0047, (2021/05/22)

The invention discloses a chiral ferrocene phosphine-indole aminophosphine ligand as well as a preparation method and application thereof. The preparation method comprises the following steps: dissolving a chiral ferrocene phosphine-indole intermediate in

P-Stereogenic N-Phosphine-Phosphite Ligands for the Rh-Catalyzed Hydrogenation of Olefins

Biosca, Maria,De La Cruz-Sánchez, Pol,Diéguez, Montserrat,Pàmies, Oscar

, p. 4730 - 4739 (2020/05/08)

We have identified a successful family of simple P-stereogenic N-phosphine-phosphite ligands for the Rh-catalyzed asymmetric hydrogenation of olefins. These catalysts show excellent enantiocontrol for α-dehydroamino acid derivatives and α-enamides (ee's u

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