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105496-34-2

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105496-34-2 Usage

Definition

ChEBI: A L-histidine derivative that is N,N-dimethyl-L-histidine substituted at positions N3 and C5 on the imidazole ring by methyl and mercapto groups respectively.

Check Digit Verification of cas no

The CAS Registry Mumber 105496-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,9 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105496-34:
(8*1)+(7*0)+(6*5)+(5*4)+(4*9)+(3*6)+(2*3)+(1*4)=122
122 % 10 = 2
So 105496-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H15N3O2S/c1-11(2)7(9(13)14)4-6-8(15)10-5-12(6)3/h5,7,15H,4H2,1-3H3,(H,13,14)/t7-/m0/s1

105496-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ovothiol C

1.2 Other means of identification

Product number -
Other names -

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:105496-34-2 SDS

105496-34-2Downstream Products

105496-34-2Related news

Heterocyclic thiols as antioxidants: Why ovothiol C (cas 105496-34-2) is a better antioxidant than ergothioneine07/14/2019

Spectral, acid-base, and redox properties of 4-mercaptoimidazoles were investigated by pulse radiolysis in aqueous solutions. Thiyl radicals of 1-methyl-5-ethyl-4-mercaptoimidazole (MEMI) have weak absorption band at 330 nm, ϵ = 300 ± 60 M−1 cm−1. Because the ionic strength variation from 0.01 ...detailed

105496-34-2Relevant articles and documents

Total Synthesis of Marine Mercaptohistidines: Ovothiols A, B, and C

Holler, Tod P.,Ruan, Fuqiang,Spaltenstein, Andreas,Hopkins, Paul B.

, p. 4570 - 4575 (2007/10/02)

Syntheses of ovothiols A and C in optically active form and ovothiols A and B in racemic form are reported.In all cases, synthesis of an S-protected mercaptoimidazole is followed by elaboration of an amino acid side chain.

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