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868696-17-7

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868696-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868696-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,9 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 868696-17:
(8*8)+(7*6)+(6*8)+(5*6)+(4*9)+(3*6)+(2*1)+(1*7)=247
247 % 10 = 7
So 868696-17-7 is a valid CAS Registry Number.

868696-17-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-phenylvinyl)-1,2,5-trioxaspiro[5.5]undecan-9-ol

1.2 Other means of identification

Product number -
Other names -

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:868696-17-7 SDS

868696-17-7Relevant articles and documents

Orally active 1,2,4-trioxanes: Synthesis and antimalarial assessment of a new series of 9-functionalized 3-(1-arylvinyl)-1,2,5-trioxaspiro[5.5]undecanes against multi-drug-resistant Plasmodium yoelii nigeriensis in mice

Singh, Chandan,Malik, Heetika,Puri, Sunil K.

, p. 2794 - 2803 (2007/10/03)

Using easily accessible keto-trioxanes 7a-g as the starting materials, a series of new variously functionalized 1,2,4-trioxanes 10-36 have been prepared and evaluated for antimalarial activity against multi-drug-resistant Plasmodium yoelii nigeriensis in

Protection of the carbonyl group as 1,2,4-trioxane and its regeneration under basic conditions

Singh, Chandan,Malik, Heetika

, p. 5673 - 5676 (2007/10/03)

(Chemical Equation Presented) An experimental protocol demonstrating the protection of the carbonyl group as 1,2,4-trioxane, the stability of the protecting group under a variety of reaction conditions, and the regeneration of the carbonyl group with Triton B in THF at room temperature is presented. The method provides a useful alternative for the protection of carbonyl compounds having acid-sensitive moieties.

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