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Glycine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-a-aspartyl]-, 4-cyclohexyl 1-(phenylmethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107164-83-0

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107164-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107164-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,6 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107164-83:
(8*1)+(7*0)+(6*7)+(5*1)+(4*6)+(3*4)+(2*8)+(1*3)=110
110 % 10 = 0
So 107164-83-0 is a valid CAS Registry Number.

107164-83-0SDS

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-Asp(OcHex)-Gly-OBzl

1.2 Other means of identification

Product number -
Other names Boc-Asp(OCHx)Gly-OBzl

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:107164-83-0 SDS

107164-83-0Relevant academic research and scientific papers

Non-linear hydrophobic-induced pKa shifts: Implications for efficiency of conversion to chemical energy

Urry, Dan W.,Gowda, D. Channe,Peng, Shao Qing,Parker, Timothy M.

, p. 67 - 74 (2007/10/02)

By using one Asp or one Glu per thirty residues in a polytricosapeptide capable of exhibiting a hydrophobic folding and assembly transition and stepwise converting a set of the five Val residues( most proximal to the Asp or Glu residue) to more-hydrophobi

Application of a unique automated synthesis system for solution-phase peptide synthesis

Sugawara,Kobayashi,Okamoto,Kitada,Fujino

, p. 1272 - 1280 (2007/10/02)

An automated synthesis system, which is suitable for repetitive syntheses using similar reaction procedures, was used to synthesize systematically a library of all possible dipeptides (25) and tripeptides (125) from 5 protected amino acids. The apparatus has also been applied to the automated synthesis of 10 fragment tripeptide derivatives that are constituents of the hormone PACAP-27. The measured molecular optical rotation values of the library of 125 tripeptides were found to correlate well with calculated values obtained by summation of the molecular optical rotation values for the constituent amino acids.

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