Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6936-65-8

Post Buying Request

6936-65-8 Suppliers

Recommended suppliersmore

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

6936-65-8 Usage

Type

Chemical compound

Derivative

Pentitol

Contains

Substituted cyclohexa-2,4-dien-1-ylidene group

Properties

Unique due to the presence of the substituted group

Potential applications

Pharmaceuticals, research, and other organic chemistry-related industries

Uses

Vary depending on the specific application

Effects

Specific interactions and effects due to the presence of the substituted group

Further research

Needed to fully understand and harness the potential of this compound

Check Digit Verification of cas no

The CAS Registry Mumber 6936-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6936-65:
(6*6)+(5*9)+(4*3)+(3*6)+(2*6)+(1*5)=128
128 % 10 = 8
So 6936-65-8 is a valid CAS Registry Number.

6936-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (6E)-6-[(2,3,4,5-tetrahydroxypentylamino)methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names Salicyliden-D-ribitylamin

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:6936-65-8 SDS

6936-65-8Downstream Products

6936-65-8Relevant articles and documents

ELECTRO-ORGANIC REACTIONS. PART 33. REDUCTION OF SUGAR OXIMES

Ryan, Gary,Utley, H. P.,Jones, Haydn F.

, p. 3699 - 3702 (2007/10/02)

Monosaccharide oximes reduce irreversibly at ca.-1.73V vs Ag/AgI in the presence of a proton donor; preparative scale constrant current electro-reduction, in aqueous solution, gives efficient conversion into the corresponding glycamines which are isolated as Schiff base or acetate derivatives.

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 6936-65-8