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133565-42-1

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133565-42-1 Usage

General Description

BOC-L-GLUTAMINOL, also known as Boc-Gln-OH, is a chemical compound commonly used in organic synthesis. It is an amino acid derivative with a Boc-protected glutamine residue, which is a common building block in peptide and protein synthesis. Boc-Gln-OH is used as a reagent in solid-phase peptide synthesis to introduce glutamine residues into the peptide chain. It is also employed in the synthesis of various pharmaceuticals, agrochemicals, and bioactive compounds. Boc-Gln-OH is typically stored and handled as a stable solid and is compatible with a wide range of solvents and reagents commonly used in organic synthesis. Overall, BOC-L-GLUTAMINOL is a valuable chemical tool in the development of new molecules and compounds in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 133565-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,6 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133565-42:
(8*1)+(7*3)+(6*3)+(5*5)+(4*6)+(3*5)+(2*4)+(1*2)=121
121 % 10 = 1
So 133565-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H20N2O4/c1-10(2,3)16-9(15)12-7(6-13)4-5-8(11)14/h7,13H,4-6H2,1-3H3,(H2,11,14)(H,12,15)/t7-/m0/s1

133565-42-1SDS

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 Boc-L-Glutaminol

1.2 Other means of identification

Product number -
Other names Boc-Glutaminol

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:133565-42-1 SDS

133565-42-1Downstream Products

133565-42-1Relevant articles and documents

STAT DEGRADERS AND USES THEREOF

-

Paragraph 00565; 00567, (2021/09/26)

The present invention provides compounds, compositions thereof, and methods of using the same.

A facile synthesis of chiral N-protected β-amino alcohols

Rodriguez,Llinares,Doulut,Heitz,Martinez

, p. 923 - 926 (2007/10/02)

Chiral N-protected β-amino alcohols are easily obtained by NaBH4 reduction of mixed anhydrides of N-protected α-amino acids in an organic/aqueous medium. The alcohols obtained from side chain or main chain reduction of N-protected aspartic acid are converted in good yields into lactones.

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