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N-ME-P-NITRO-PHE-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70663-55-7

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70663-55-7 Usage

Chemical Properties

White to light yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 70663-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,6 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70663-55:
(7*7)+(6*0)+(5*6)+(4*6)+(3*3)+(2*5)+(1*5)=127
127 % 10 = 7
So 70663-55-7 is a valid CAS Registry Number.

70663-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ME-P-NITRO-PHE-OH

1.2 Other means of identification

Product number -
Other names H-L-MEPHE(4-NO2)-OH

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:70663-55-7 SDS

70663-55-7Upstream product

70663-55-7Downstream Products

70663-55-7Relevant academic research and scientific papers

Mechanistic Investigation of Phenylalanine Ammonia Lyase by Using N-Methylated Phenylalanines

Viergutz, Sandra,Poppe, Laszlo,Tomin, Anna,Retey, Janos

, p. 3601 - 3612 (2007/10/03)

N-Methyl-L-phenylalanine (5), N-methyl-4-nitro-L-phenylalanine (6), and N,N-dimethyl-4-nitro-L-phenyl-alanine (7·H+) were investigated as substrates of inhibitors of phenylalanine ammonia lyase from Petroselinum crispum. Whereas the former was

Synthesis, opiate receptor binding and analgesic activity of enkephalin analogues

Pless,Bauer,Cardinaux,et al.

, p. 398 - 411 (2007/10/16)

The synthesis and biological testing of analogues of Met-enkephalin, a recently discovered opioid peptide from mammalian brain, are described. Testing involved determination of affinity constants for an opiate receptor site and of analgesic potency in the tail-flick test in mouse. The effects on opioid activity on modifying various parts of the enkephalin molecule are discussed. Tyr-D-Ala-Gly-MePhe-Met(O)-ol1) (FK 33-824), which was highly active in these tests, was subsequently selected for clinical testing. The use of two complementary models - in vitro binding studies and in vivo test for analgesia - for the assessment of biological activity in the evaluation of analogues is explained.

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