Welcome to LookChem.com Sign In|Join Free
  • or
2-C-Methyl-myo-inositol, also known as 2-C-methyl-D-myo-inositol or 2-C-methyl-myo-inositol, is a naturally occurring organic compound that belongs to the inositol family. It is a cyclohexane hexol, meaning it has a six-membered ring structure with six hydroxyl groups and one methyl group attached to the second carbon. 2-C-Methyl-myo-inositol plays a significant role in various biological processes, including cell signaling and membrane function. It can be found in plants, animals, and microorganisms, and has been studied for its potential therapeutic applications in treating certain diseases and conditions. 2-C-Methyl-myo-inositol is also used as a research tool in scientific studies to understand the role of inositol in cellular processes and its impact on human health.

472-96-8

Post Buying Request

472-96-8 Suppliers

Recommended suppliers

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

472-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 472-96-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 472-96:
(5*4)+(4*7)+(3*2)+(2*9)+(1*6)=78
78 % 10 = 8
So 472-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O6/c1-7(13)5(11)3(9)2(8)4(10)6(7)12/h2-6,8-13H,1H3

472-96-8SDS

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 MYO-INOSITOL, 2-C-METHYL-

1.2 Other means of identification

Product number -
Other names 2-C-Methyl-myo-inosit

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:472-96-8 SDS

472-96-8Relevant academic research and scientific papers

The orientation of the β-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes

Jagdhane, Rajendra C.,Patil, Madhuri T.,Krishnaswamy, Shobhana,Shashidhar, Mysore S.

, p. 5144 - 5151 (2013/06/27)

A comparison of the results of the Grignard reaction and the hydride reduction of the carbonyl group of epi- and scyllo-inososes reveals that the extent of diastereoselectivity of these reactions is decided by the orientation of the β-hydroxyl group (or i

Sulfonate protecting groups. Synthesis of O- and C-methylated inositols: D- and L-ononitol, D- and L-laminitol, mytilitol and scyllo-inositol methyl ether

Sarmah, Manash P.,Shashidhar, Mysore S.,Sureshan, Kana M.,Gonnade, Rajesh G.,Bhadbhade, Mohan M.

, p. 4437 - 4446 (2007/10/03)

Syntheses of d- and l-ononitol, d- and l-laminitol, mytilitol and scyllo-inositol methyl ether starting from myo-inositol are described. One or two of the myo-inositol 1,3,5-orthoformate hydroxyl groups were protected as tosylates. These mono or ditosylat

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 472-96-8