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305-96-4

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305-96-4 Usage

Chemical Properties

White to Off-White Solid

Uses

Different sources of media describe the Uses of 305-96-4 differently. You can refer to the following data:
1. It maybe of therapeutic value in the treatment of Parkinsonism
2. A Phenylalanine (P319415) analog
3. A Phenylalanine (P319415) analog.

Check Digit Verification of cas no

The CAS Registry Mumber 305-96-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 305-96:
(5*3)+(4*0)+(3*5)+(2*9)+(1*6)=54
54 % 10 = 4
So 305-96-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c1-10(11,9(13)14)6-7-3-2-4-8(12)5-7/h2-5,12H,6,11H2,1H3,(H,13,14)/t10-/m0/s1

305-96-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name α-Methyl-D,L-m-tyrosine

1.2 Other means of identification

Product number -
Other names DL-ALPHA-METHYL-M-TYROSINE MONOHYDRATE

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:305-96-4 SDS

305-96-4Downstream Products

305-96-4Relevant articles and documents

α-METHYL AMINO ACIDS BY CATALYTIC PHASE-TRANSFER ALKYLATIONS

O'Donnell, Martin J.,LeClef, Brigitte,Rusterholz, David B.,Ghosez, Leon,Antoine, Jean-Pierre,Navarro, Mirtha

, p. 4259 - 4262 (2007/10/02)

The α-methyl amino acids, α-methyl p-chlorophenylalanine, α-methyl p-tyrosine, α-methyl m-tyrosine and α-methyl DOPA have been prepared in good yields from amino ester hydrochlorides.The key step in the method is the catalytic phase-transfer alkylation of Schiff base derivatives of monoalkyl amino acids.

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