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822-83-3

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822-83-3 Usage

Definition

ChEBI: A dioxolane that is 1,3-dioxolane substituted by an isopropyl group at position 2.

Check Digit Verification of cas no

The CAS Registry Mumber 822-83-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 822-83:
(5*8)+(4*2)+(3*2)+(2*8)+(1*3)=73
73 % 10 = 3
So 822-83-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2/c1-5(2)6-7-3-4-8-6/h5-6H,3-4H2,1-2H3

822-83-3SDS

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 2-isopropyl-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 2-propan-2-yl-1,3-dioxolane

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:822-83-3 SDS

822-83-3Relevant articles and documents

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Gatti,Morandi

, p. 4393 (1965)

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Synthesis of ethers and cyclic acetals in the presence of CBV-720 zeolite

Baiburtli,Raskil’dina,Zlotskii

, p. 1098 - 1101 (2017/11/22)

СBV-720 zeolite was compared to H-Beta zeolite and KU-2 cation-exchange resin in the catalytic performance in addition of alcohols to norbornene, in condensation of aldehyde and ketone with di- and triols, and in the Prins reaction of olefins with formaldehyde. These reactions, when performed on СBV-720 zeolite, occur 1.5–2 times faster than on the other catalysts. The corresponding ethers and cyclic acetals were synthesized.

Bis(perfluorooctanesulfonyl)imide supported on fluorous silica gel: Application to protection of carbonyls

Hong, Mei,Xiao, Guomin

experimental part, p. 121 - 126 (2012/08/28)

The immobilization of bis(perfluorooctanesulfonyl)imide (HNPf2) on fluorous silica gel (FSG) and its utilization in protection of carbonyls have been investigated. This system is reasonably general and can be applied to converting several carbonyls to the corresponding acetals and ketals in good to excellent yields. There is no need for the use of anhydrous solvents or inert atmosphere. Recycling studies have shown that the FSG-supported HNPf2 catalyst can be readily recovered and reused several times without significant loss of activity.

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