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122532-80-3

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122532-80-3 Usage

General Description

BOC-LYS(2-PICOLINOYL)-OH, also known as N_ε-tert-butoxycarbonyl-L-lysine(2-picolinoyl)-OH, is a chemical compound used in the field of organic chemistry and drug development. It is a derivative of lysine, an essential amino acid, and features a Boc (tert-butoxycarbonyl) protective group as well as a 2-picolinoyl group. BOC-LYS(2-PICOLINOYL)-OH is often used as a building block in the synthesis of peptide-based drugs and pharmaceuticals due to its ability to introduce lysine residues into peptide sequences. It is also used as a tool in the study of protein-protein interactions and post-translational modifications. Overall, BOC-LYS(2-PICOLINOYL)-OH plays a crucial role in the development of novel therapeutic compounds and in biochemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 122532-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,5,3 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122532-80:
(8*1)+(7*2)+(6*2)+(5*5)+(4*3)+(3*2)+(2*8)+(1*0)=93
93 % 10 = 3
So 122532-80-3 is a valid CAS Registry Number.

122532-80-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-LYS(2-PICOLINOYL)-OH

1.2 Other means of identification

Product number -
Other names BOC-LYSINE(2-PICOLINOYL)-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:122532-80-3 SDS

122532-80-3Downstream Products

122532-80-3Relevant articles and documents

Decreased histamine release by luteinizing hormone-releasing hormone antagonists obtained upon translocation of the cationic amino acid from position 8 to position 7

Flouret,Mahan,Majewski

, p. 636 - 640 (2007/10/02)

We report analogues of N-Ac-D-Nal-D-Cpa-D-Pal-Ser-Lys(Pic)-D-Lys(Pic)-Leu- Ilys-Pro-D-Ala-NH2, the parent antagonist (PA), which is a potent antagonist of LHRH. To simplify future radioactive labeling we prepared N-Ac-D-Nal-D- Cpa-D-Pal-Ser-Lys

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