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L-Alanine, N-[N-[N-[(phenylmethoxy)carbonyl]-L-a-aspartyl]-L-seryl]-, 4-(phenylmethyl) ester, 1-[2-[(1,1-dimethylethoxy)carbonyl]hydrazide] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63589-70-8

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63589-70-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63589-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,8 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63589-70:
(7*6)+(6*3)+(5*5)+(4*8)+(3*9)+(2*7)+(1*0)=158
158 % 10 = 8
So 63589-70-8 is a valid CAS Registry Number.

63589-70-8SDS

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 Z-Asp(OCH2Ph)-Ser-AlaNHNH-Boc

1.2 Other means of identification

Product number -
Other names (S)-3-Benzyloxycarbonylamino-N-{(S)-1-[(S)-2-(N'-tert-butoxycarbonyl-hydrazino)-1-methyl-2-oxo-ethylcarbamoyl]-2-hydroxy-ethyl}-succinamic acid benzyl ester

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:63589-70-8 SDS

63589-70-8Upstream product

63589-70-8Downstream Products

63589-70-8Relevant academic research and scientific papers

Synthesis of phenolic group containing analogues of porcine secretin and their immunological properties

Yanaihara,Kubota,Sakagami,Sato,Mochizuki

, p. 648 - 655 (2007/10/06)

Syntheses by the conventional method are described of Nα-tyrosylsecretin, [Tyr1]secretin, and Nα-β-(4-hydroxyphenyl)propionylsecretin. Secretin and [Tyr6] secretin were also prepared by the synthetic route identical with those employed for construction of the above analogues. Purification of secretin and the analogues was conducted by ion-exchange column chromatography on CM-Sephadex and gel filtration. Immunological reactivities of these analogues were examined in the radioimmunoassay system for secretin using two different antisera raised against synthetic secretin in rabbits. The tracers used in this study were [125I]-[Tyr1] secretin and [125I]-[Tyr6]secretin. The dose-response curves of Nα-tyrosylsecretin, [Tyr1]secretin, and Nα-β-(4-hydroxyphenyl) propionylsecretion were essentially superimposable upon those of natural and synthetic preparations of porcine secretin in the systems used, while [Tyr6]secretin showed discrepancy in the curve. In addition, biological activities of the synthetic polypeptides were compared with that of natural porcine secretin in terms of exocrine pancreatic secretory response in anesthetized dogs.

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