Welcome to LookChem.com Sign In|Join Free

CAS

  • or

85013-25-8

Post Buying Request

85013-25-8 Suppliers

Recommended suppliersmore

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

85013-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85013-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,1 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85013-25:
(7*8)+(6*5)+(5*0)+(4*1)+(3*3)+(2*2)+(1*5)=108
108 % 10 = 8
So 85013-25-8 is a valid CAS Registry Number.

85013-25-8SDS

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 n-propyl-3,4-dichlorophenyltriazene

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:85013-25-8 SDS

85013-25-8Upstream product

85013-25-8Relevant articles and documents

Substituent Effects on Tautomerisation Constants of Alkylaryltriazenes

Kelly, Miguel A.,Murray, Martin,Sinnott, Michael L.

, p. 1649 - 1654 (2007/10/02)

Both tautomers of propyl-p-nitrophenyl-, -p-cyanophenyl-, -3,5-dichlorophenyl-, and -p-chlorophenyl-triazenes are directly observable by 1H n.m.r. at 200 MHz in CD3CN at 25 deg C.In addition, lower temperature studies enable the two tautomers of propyl-p-methylphenyl- and -p-methoxyphenyl-triazenes to be quantitated.At -45 deg C rotamers about the N-N bond of the conjugated tautomers are also separately observable. 13C N.m.r. studies of the p-nitro- and p-chloro-compounds suggest tautomerisation involves the less abundant rotamer of the conjugated tautomer and the unconjugated tautomer.The position of equilibrium at 25 deg C is described by log (/) = (0.67 +/- 0.13) - (0.31 +/- 0.04)pKa (ArNH3+). 13C, as well as 1H n.m.r. studies indicate that change of solvent to (CD3)2SO, CD3CN-(CD3)2SO, or CD3CN-(CD3)2SO-H2O has little effect.Neither, in the p-nitrophenyl case, does change of the propyl group for benzyl.

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 85013-25-8