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98708-79-3

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98708-79-3 Usage

General Description

DL-p-Isopropylphenylalanine is a chemical compound with the molecular formula C12H15NO2. It is a derivative of phenylalanine, containing an isopropyl group attached to the para position of the phenyl ring. DL-p-Isopropylphenylalanine is commonly used as a building block in the synthesis of peptides and proteins, as well as in the production of pharmaceuticals. It is also known for its potential use in the development of drugs for the treatment of neurological disorders and psychiatric conditions. Additionally, DL-p-Isopropylphenylalanine has been studied for its role in regulating neurotransmitter levels in the brain, making it a potential target for drug development in the field of neuroscience.

Check Digit Verification of cas no

The CAS Registry Mumber 98708-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,0 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98708-79:
(7*9)+(6*8)+(5*7)+(4*0)+(3*8)+(2*7)+(1*9)=193
193 % 10 = 3
So 98708-79-3 is a valid CAS Registry Number.

98708-79-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-3-(4-propan-2-ylphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 2-AMINO-3-(4-ISOPROPYLPHENYL)PROPANOIC ACID

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:98708-79-3 SDS

98708-79-3Upstream product

98708-79-3Downstream Products

98708-79-3Relevant articles and documents

Organocatalytic Enantioselective Addition of α-Aminoalkyl Radicals to Isoquinolines

Liu, Xiangyuan,Liu, Yang,Chai, Guobi,Qiao, Baokun,Zhao, Xiaowei,Jiang, Zhiyong

supporting information, p. 6298 - 6301 (2018/10/09)

With a dual organocatalytic system involving a chiral phosphoric acid and a dicyanopyrazine-derived chromophore (DPZ) photosensitizer and under the irradiation with visible light, an enantioselective Minisci-type addition of α-amino acid-derived redox-active esters (RAEs) to isoquinolines has been developed. A variety of prochiral α-aminoalkyl radicals generated from RAEs were successfully introduced on isoquinolines, providing a range of valuable α-isoquinoline-substituted chiral secondary amines in high yields with good to excellent enantioselectivities.

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