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BOC-D-CYS(BZL)-OH is a chemical compound utilized in scientific and pharmacological research, particularly in the domain of peptide synthesis. It is a variant of the amino acid cysteine, featuring a Benzyl (BZL) and tert-Butyloxycarbonyl (BOC) protecting groups. The BOC group serves to shield the compound during peptide synthesis, ensuring its stability and reactivity in the creation of more complex molecules. BOC-D-CYS(BZL)-OH is a valuable asset in the development of innovative drugs and therapeutics, being widely employed by researchers across the globe.

102830-49-9

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102830-49-9 Usage

Uses

Used in Pharmaceutical Research:
BOC-D-CYS(BZL)-OH is used as a precursor in the synthesis of peptides for pharmaceutical applications. Its role is crucial in the development of new drugs and therapies, as it contributes to the formation of complex molecular structures that can target specific biological processes.
Used in Scientific Research:
In the field of scientific research, BOC-D-CYS(BZL)-OH is employed as a building block for creating intricate molecular constructs. Its presence in peptide synthesis allows for the exploration of novel chemical interactions and the potential discovery of new biological functions.
Used in Drug Development:
BOC-D-CYS(BZL)-OH is used as a key component in drug development, where its protective groups facilitate the synthesis of peptides with desired properties. The removal of the BOC group in later stages of the process enables the compound to participate in crucial biological activities, making it an essential tool in the creation of effective treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 102830-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,3 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102830-49:
(8*1)+(7*0)+(6*2)+(5*8)+(4*3)+(3*0)+(2*4)+(1*9)=89
89 % 10 = 9
So 102830-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H21NO4S/c1-15(2,3)20-14(19)16-12(13(17)18)10-21-9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m1/s1

102830-49-9 Well-known Company Product Price

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  • Aldrich

  • (98920)  Boc-D-Cys(Bzl)-OH  ≥99.0%

  • 102830-49-9

  • 98920-1G-F

  • 760.50CNY

  • Detail

102830-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Boc-S-benzyl-D-cysteine

1.2 Other means of identification

Product number -
Other names (2S)-3-benzylsulfanyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]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:102830-49-9 SDS

102830-49-9Relevant academic research and scientific papers

Combination of non-natural D-amino acid derivatives and allophenylnorstatine-dimethylthioproline scaffold in HIV protease inhibitors have high efficacy in mutant HIV

Nakatani, Shingo,Hidaka, Koushi,Ami, Ei'Ichi,Nakahara, Koichiro,Sato, Akihiko,Nguyen, Jeffrey-Tri,Hamada, Yoshio,Hori, Yasuko,Ohnishi, Nobuyuki,Nagai, Akinori,Kimura, Tooru,Hayashi, Yoshio,Kiso, Yoshiaki

experimental part, p. 2992 - 3004 (2009/04/05)

Several non-natural D-amino acid derivatives were introduced as P2/P3 residues in allophenylnorstatine-containing (Apns; (2S,3S)-3-amino-2-hydroxy-4- phenylbutyric acid) HIV protease inhibitors. The synthetic analogues exhibited potent inhibitory activity

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