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74193-68-3

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  • L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-, phenylmethyl ester

    Cas No: 74193-68-3

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74193-68-3 Usage

General Description

L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-, phenylmethyl ester is a chemical compound that is a derivative of L-leucine and L-phenylalanine. It is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and peptides. L-Leucine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-, phenylmethyl ester is known for its ability to enhance protein synthesis and muscle growth, making it a popular ingredient in sports supplements and performance-enhancing products. Additionally, it has been studied for its potential role in improving insulin sensitivity and managing metabolic disorders. However, its safety and efficacy for these purposes are still being researched.

Check Digit Verification of cas no

The CAS Registry Mumber 74193-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,9 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74193-68:
(7*7)+(6*4)+(5*1)+(4*9)+(3*3)+(2*6)+(1*8)=143
143 % 10 = 3
So 74193-68-3 is a valid CAS Registry Number.

74193-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-Phe-Leu-OBn

1.2 Other means of identification

Product number -
Other names BocPheLeuOBzl

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:74193-68-3 SDS

74193-68-3Relevant articles and documents

NDTP Mediated Direct Rapid Amide and Peptide Synthesis without Epimerization

Bao, Guangjun,He, Zeyuan,Li, Jingyue,Li, Yiping,Liu, Yuyang,Ma, Wen,Sun, Wangsheng,Wang, Peng,Wang, Rui,Xie, Junqiu,Yu, Changjun

supporting information, (2022/01/28)

Herein, we explored an unprecedented mild, nonirritating, conveniently available, and recyclable coupling reagent NDTP, which could activate the carboxylic acids via acyl thiocyanide and enable the rapid amide and peptide synthesis at very mild conditions

The photoredox-catalyzed hydrosulfamoylation of styrenes and its application in the novel synthesis of naratriptan

Chen, Miaomiao,Ding, Xin,Gao, Yongyue,He, Xingxing,Kang, Jin,Lu, Aidang,Wang, Qingmin,Wang, Ziwen,Zhang, Mingjun

supporting information, p. 9140 - 9143 (2021/09/14)

The hydrosulfamoylation of diverse aryl olefins provides facile access to alkylsulfonamides. Here we report a novel protocol utilizing radical-mediated addition and a thiol-assisted strategy to achieve the hydrosulfamoylation of diverse styrenes in modest to excellent yields under mild and economic reaction conditions. The methodology was found to provide an efficient and convenient approach for the synthesis of the anti-migraine drug naratriptan and it also can be used for the late-stage functionalization of natural products or medicines.

Naphthoquinones as covalent reversible inhibitors of cysteine proteases—studies on inhibition mechanism and kinetics

Barthels, Fabian,Distler, Ute,Engel, Volker,Engels, Bernd,Hellmich, Ute A.,Johe, Patrick,Klein, Philipp,Le, Thien Anh,Opatz, Till,Schirmeister, Tanja,Schmid, Paul,Tenzer, Stefan,Wagner, Annika

supporting information, (2020/05/16)

The facile synthesis and detailed investigation of a class of highly potent protease inhibitors based on 1,4‐naphthoquinones with a dipeptidic recognition motif (HN‐L‐Phe‐L‐Leu‐OR) in the 2‐position and an electron‐withdrawing group (EWG) in the 3‐positio

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