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218608-82-3

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218608-82-3 Usage

Uses

Boc-l-beta-homoisoleucine

Check Digit Verification of cas no

The CAS Registry Mumber 218608-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,6,0 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 218608-82:
(8*2)+(7*1)+(6*8)+(5*6)+(4*0)+(3*8)+(2*8)+(1*2)=143
143 % 10 = 3
So 218608-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H23NO4/c1-6-8(2)9(7-10(14)15)13-11(16)17-12(3,4)5/h8-9H,6-7H2,1-5H3,(H,13,16)(H,14,15)/t8-,9-/m1/s1

218608-82-3SDS

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-L-β-homoisoleucine

1.2 Other means of identification

Product number -
Other names Boc-L-beta-homoisoleucine

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:218608-82-3 SDS

218608-82-3Downstream Products

218608-82-3Relevant articles and documents

Protein-protein interface mimicry by an oxazoline piperidine-2,4-dione

Li, Xun,Taechalertpaisarn, Jaru,Xin, Dongyue,Burgess, Kevin

supporting information, p. 632 - 635 (2015/03/05)

Representative minimalist mimics 1 were prepared from amino acids. Scaffold 1 was not designed to mimic any particular secondary structure, but simulated accessible conformations of this material were compared with common ideal secondary structures and with >125000 different protein-protein interaction (PPI) interfaces. This data mining exercise indicates that scaffolds 1 can mimic features of sheet-turn-sheets, somewhat fewer helical motifs, and numerous PPI interface regions that do not resemble any particular secondary structure.

Wolff rearrangement of Nα-Boc-/Z-protected aminodiazoketones to the corresponding β-amino acids under microwave irradiation

Kantharaju,Patil, Basanagoud S.,Suresh Babu, Vommina V.

, p. 2611 - 2613 (2007/10/03)

The Wolff rearrangement of Nα-Boc-/Z-protected aminodiazoketones in the presence of silver benzoate under microwave irradiation is described. The reaction is found to be rapid, efficient and complete. It results in the isolation of Boc-/Z- prot

Homologation of α-amino acids to β-amino acids using Boc2O

Vasanthakumar, Ganga-Ramu,Patil, Basanagoud S.,Suresh Babu, Vommina V.

, p. 2087 - 2089 (2007/10/03)

The use of Boc2O as a coupling agent in the homologation of N-urethane protected-α-amino acid to its β-homomers by the Arndt-Eistert method is described. The homologation gives good yields without racemization. The use of Boc2O as a

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