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29709-67-9

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29709-67-9 Usage

Physical State

Colorless liquid

Solvent Usage

Used as a solvent in various chemical processes

Pharmaceutical Production

Utilized in the production of pharmaceuticals

Intermediate Synthesis

Serves as an intermediate in the synthesis of other chemical compounds

Toxicity

Considered to have low toxicity

Health Risks

Does not pose significant health risks under normal handling and use conditions

Safety

Important to handle with care and follow all safety procedures when working with it

Check Digit Verification of cas no

The CAS Registry Mumber 29709-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,0 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29709-67:
(7*2)+(6*9)+(5*7)+(4*0)+(3*9)+(2*6)+(1*7)=149
149 % 10 = 9
So 29709-67-9 is a valid CAS Registry Number.

29709-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1,2-bis(2,2-dimethyl-1,3-dioxolan-4-yl)ethanol

1.2 Other means of identification

Product number -
Other names 3-amino-3-deoxy-1,2:5,6-di-O-isopropylidene-D-altriol

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:29709-67-9 SDS

29709-67-9Relevant articles and documents

CYCLIC SULFATES CONTAINIMNG ACID-SENSITIVE GROUPS AND CHEMOSELECTIVE HYDROLYSIS OF SULFATE ESTERS

Kim, B. Moon,Sharpless, K. Barry

, p. 655 - 658 (2007/10/02)

Diols containing acid-sensitive functionalities such as acetonide and silyloxy groups are efficiently converted to the corresponding cyclic sulfates via formation of the cyclic sulfites in the presence of a base and oxidation of the isolated sulfites usin

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