Welcome to LookChem.com Sign In|Join Free

CAS

  • or

33471-33-9

Post Buying Request

33471-33-9 Suppliers

Recommended suppliersmore

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

33471-33-9 Usage

Biochem/physiol Actions

Metabolite of inositol metabolic pathways

Check Digit Verification of cas no

The CAS Registry Mumber 33471-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,7 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33471-33:
(7*3)+(6*3)+(5*4)+(4*7)+(3*1)+(2*3)+(1*3)=99
99 % 10 = 9
So 33471-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-5,7-11H/t1-,2-,3-,4+,5-/m0/s1

33471-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexan-1-one

1.2 Other means of identification

Product number -
Other names (+-)-2r,3c,4c,5t,6c-Pentahydroxy-cyclohexanon

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:33471-33-9 SDS

33471-33-9Relevant articles and documents

Protecting group directed stereoselective reduction of an epi-inosose: Efficient synthesis of epi-inositol

Patil, Madhuri T.,Krishnaswamy, Shobhana,Sarmah, Manash P.,Shashidhar, Mysore S.

supporting information; experimental part, p. 3756 - 3758 (2011/08/06)

A facile and high yielding synthesis of epi-inositol via stereoselective reduction of a pentaprotected epi-inosose is reported. Extent of stereoselectivity during the hydride reduction appears to depend on the ability of the substrate to complex with metal ions in the reducing agent.

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 33471-33-9