Welcome to LookChem.com Sign In|Join Free

CAS

  • or

89188-91-0

Post Buying Request

89188-91-0 Suppliers

Recommended suppliersmore

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

89188-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89188-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,8 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89188-91:
(7*8)+(6*9)+(5*1)+(4*8)+(3*8)+(2*9)+(1*1)=190
190 % 10 = 0
So 89188-91-0 is a valid CAS Registry Number.

89188-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name octan-4-one phenylhydrazone

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:89188-91-0 SDS

89188-91-0Relevant articles and documents

Regioselective Indolization of Unsymmetrical Phenylhydrazones by Reaction, at Room Temperature, with PCl3

Baccolini, Graziano,Bartoli, Giuseppe,Marotta, Emanuela,Todesco, Paolo E.

, p. 2695 - 2697 (2007/10/02)

Unsymmetrical ketone phenylhydrazones (1) (R1 ae R2) react with PCl3, at room temperature to give predominantly one, (2), of the two possible 2,3-disubstituted indoles in good to excellent overall yield.When the R1 and R2 groups are very different (R1 = Ph or Me; R2 = alkyl or H) the reaction is highly regioselective leading to exclusive or prevalent formation of the corresponding 3-R1 indoles (2), whereas when R1 and R2 are very similar (R1, R2 = alkyl chains) the regioselectivity is decreased and the indole having the shorter chain in the 3-position predominates, but only slightly.Inspection of the results enables the direction of indolization to be predicted and the positions of the substituents in the 2,3-disubstituted indoles to be assigned with certainty, features not inherent in the classical Fischer indolization.

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 89188-91-0