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115054-62-1

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115054-62-1 Usage

Uses

Methyldopa angiotensin II analog.

Check Digit Verification of cas no

The CAS Registry Mumber 115054-62-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,5 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115054-62:
(8*1)+(7*1)+(6*5)+(5*0)+(4*5)+(3*4)+(2*6)+(1*2)=91
91 % 10 = 1
So 115054-62-1 is a valid CAS Registry Number.

115054-62-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name L-α-Methyl DOPA Methyl Ester Hydrochloride

1.2 Other means of identification

Product number -
Other names methyl (2S)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoate,hydrochloride

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:115054-62-1 SDS

115054-62-1Relevant articles and documents

Renal-selective prodrugs for control of renal sympathetic nerve activity in the treatment of hypertension

-

Page/Page column 66-67, (2010/11/30)

Renal-selective prodrugs are described which are preferentially converted in the kidney to compounds capable of inhibiting synthesis of catecholamine-type neurotransmitters involved in renal sympathetic nerve activity. The prodrugs described herein are de

A facile method for the side-chain protection of α-methyl-β-3,4-dihydroxyphenyl-L-alanine (αMeDopa) for solid-phase peptide synthesis

Hsieh,deMaine

, p. 59 - 62 (2007/10/02)

Two approaches have been used to prepare N(α)-tert-butoxycarbonyl-α-methyl-β-3,4-dimethoxy-, or dibenzyloxyphenyl-L-alanine, N(α)-Boc-α-MeDopa(R)2, where R is the methyl or benzyl ether. In the first approach, α-methyl-β-3,4-dihydroxyphenyl-L-a

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