Welcome to LookChem.com Sign In|Join Free

CAS

  • or

85313-58-2

Post Buying Request

85313-58-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

85313-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85313-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,1 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85313-58:
(7*8)+(6*5)+(5*3)+(4*1)+(3*3)+(2*5)+(1*8)=132
132 % 10 = 2
So 85313-58-2 is a valid CAS Registry Number.

85313-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name t-Bumeoc-L-Phe-D-Leu-L-Arg-L-Phe-NH2

1.2 Other means of identification

Product number -
Other names ((S)-1-{(R)-1-[(S)-1-((S)-1-Carbamoyl-2-phenyl-ethylcarbamoyl)-4-guanidino-butylcarbamoyl]-3-methyl-butylcarbamoyl}-2-phenyl-ethyl)-carbamic acid 1-(3,5-di-tert-butyl-phenyl)-1-methyl-ethyl ester

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:85313-58-2 SDS

85313-58-2Downstream Products

85313-58-2Relevant articles and documents

The 1-(3,5-Di-tert-butylphenyl)-1-methylethoxycarbonyl (t-Bumeoc) Residue, a Protecting Group Cleavable under Extremely Mild Acidic Conditions

Voelter, Wolfgang,Mueller, Juergen

, p. 248 - 260 (2007/10/02)

The synthesis of 1-(3,5-di-tert-butylphenyl)-1-methylethoxycarbonyl fluoride (8) and its reaction with selected amino acids as well as the 13C NMR spectroscopic characterization of t-Bumeoc derivatives are described.The new protecting group is cleavable under very mild acidic conditions.The kinetics of the cleavage is studied by high-performance liquid chromatography (HPLC).The utility of the t-Bumeoc compared to the Adpoc protecting group is demonstrated taking a derivative of the molluscan neuropeptide as an example.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 85313-58-2