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650624-42-3

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650624-42-3 Usage

General Description

L-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl-L-seryl-, methyl ester is a chemical compound with a complex molecular structure. It is a methyl ester derivative of the amino acids leucine, tyrosine, and serine. L-Leucine, N-[(1,1-dimethylethoxy)carbonyl]-L-tyrosyl-L-seryl-, methyl ester is primarily used in research and pharmaceutical applications for its potential in protein synthesis and regulation. It is also used in the development of new drugs and therapeutics, particularly in the field of oncology and immunology. Additionally, this compound has shown potential in enhancing muscle growth and repair, making it a promising candidate for use in sports nutrition and supplements.

Check Digit Verification of cas no

The CAS Registry Mumber 650624-42-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,0,6,2 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 650624-42:
(8*6)+(7*5)+(6*0)+(5*6)+(4*2)+(3*4)+(2*4)+(1*2)=143
143 % 10 = 3
So 650624-42-3 is a valid CAS Registry Number.

650624-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-Tyr-Ser-Leu-OMe

1.2 Other means of identification

Product number -
Other names (S)-2-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-hydroxy-propionylamino}-4-methyl-pentanoic acid methyl 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:650624-42-3 SDS

650624-42-3Downstream Products

650624-42-3Relevant articles and documents

The synthesis, distribution, and anti-hepatic cancer activity of YSL

Ding, Wenfeng,Zhang, Jiali,Yao, Zhi,Lu, Rong,Wu, Dezhu,Li, Ginfu,Shen, Zilong,Sun, Yingji,Lin, Gang,Wang, Chao,Zhao, Ming,Peng, Shiqi

, p. 4989 - 4994 (2007/10/03)

(I) HCl/CH3OH; (II) DCC/HOBt/NMM with corresponding carboxyl component; (III) HCl/CH3CO2C2H5 (6 mol/L); (IV) NaOH/H2O/CH3OH; (V) 3H2 and 10% Pd/C. YSL was prepared stepwise from C terminal to N terminal with the side chain un-protective amino acids, Boc-Leu-OMe, Boc-Ser-OH, and Boc-Tyr-OH, as the starting materials in 39.5% total yield (31.2 g/per batch). With the side chain un-protective Boc-(3,5-dibromo)-Tyr-OH and HClA·Ser-Leu-OMe as the starting materials (3,5-3H-Tyr)-Ser-Leu-OH was obtained in 29% yield. The determination of radioactive quantity in the urine and feces indicated that even after the administration for 130 h only 8.4% (5.35% in urine and 3.05% in feces) of total radioactive quantity from the metabolite of [3,5-3H-Tyr]-Ser-Leu-OH were monitored. The distribution study revealed the relative accumulation level of the individual tissue was arranged in the sequence of spleen > liver > kidney > lung > heart > muscle > brain. Selecting hepatic cancer as the target YSL significantly increased the survival time of H22 tumor cells implanted mice.

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