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128525-54-2

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128525-54-2 Usage

Chemical compound

Derived from camphor and myo-inositol

Physical state

Solid

Color

White

Crystalline structure

Crystalline

Solubility

Sparingly soluble in water

Potential use

Pharmaceutical industry

Application

Chiral auxiliary in organic synthesis

Investigation

Building block in the synthesis of various bioactive compounds

Chirality

Chiral compound

Utility

Utilized in asymmetric synthesis

Significance

Produces enantiomerically pure compounds

Importance

Important tool in the field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 128525-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,5,2 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128525-54:
(8*1)+(7*2)+(6*8)+(5*5)+(4*2)+(3*5)+(2*5)+(1*4)=132
132 % 10 = 2
So 128525-54-2 is a valid CAS Registry Number.

128525-54-2SDS

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 1,2-O-CAMPHANYLIDENE-L-MYO-INOSITOL

1.2 Other means of identification

Product number -
Other names 1,2-O-CAMPHANYLIDENE-L-MYO-INOSITOL

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:128525-54-2 SDS

128525-54-2Downstream Products

128525-54-2Relevant articles and documents

Efficient and systematic syntheses of enantiomerically pure and regiospecifically protected myo-inositols

Bruzik, Karol S.,Tsai, Ming-Daw

, p. 6361 - 6374 (2007/10/02)

Efficient and systematic syntheses of a variety of enantiomerically pure and regiospecifically protected myo-inositols, which can be readily used as precursors for most natural and unnatural derivatives of myo-inositol, have been developed. The key strate

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