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3962-41-2

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3962-41-2 Usage

Type of compound

Synthetic organic compound

Structure

Cyclic ketone derivative with a dioxane ring and two carbonyl groups

Applications

a. Organic synthesis
b. Pharmaceutical research (as a building block and intermediate)
c. Development of new materials and polymers (due to unique chemical structure)

Precaution

Potential health and environmental hazards; handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 3962-41-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,6 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3962-41:
(6*3)+(5*9)+(4*6)+(3*2)+(2*4)+(1*1)=102
102 % 10 = 2
So 3962-41-2 is a valid CAS Registry Number.

3962-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-benzhydryl-2,2-dimethyl-1,3-dioxane-4,6-dione

1.2 Other means of identification

Product number -
Other names 5-benzhydryl-2,2-dimethyl-[1,3]dioxane-4,6-dione

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:3962-41-2 SDS

3962-41-2Relevant articles and documents

Fe(HSO4)3 : An efficient, heterogeneous and reusable catalyst for C-alkylation of β-dicarbonyl compounds

Khafajeh, Samaneh,Akhlaghinia, Batool,Rezazadeh, Soodabeh,Eshghi, Hossein

, p. 1903 - 1912 (2015/02/05)

Fe(HSO4)3(FHS) was used as an efficient catalyst for the heterogeneous addition of a series of benzylic and allylic alcohols to various β-dicarbonyl compounds, which afforded moderate to excellent yields of C-alkylated products in 1,2-dichloroethane. In comparison with the previous methods, the present research surprisingly exhibited higher reaction yields without formation of any by-products which could be formed by self-condensation of alcohols. Moreover, the catalyst can be readily recovered and reused up to five times with almost maintained reactivity and yields.

ONE POT SYNTHESIS OF MONOSUBSTITUTED ISOPROPYLIDENE MALONATES

Huang, Xian,Xie, Linghong

, p. 1701 - 1708 (2007/10/02)

Monosubstituted isopropylidene malonates have been synthesized from Meldrum's acid and carbonyl compounds in the presence of sodium hydrogentelluride as a one pot reaction.

CONJUGATE ADDITION OF GRIGNARD REAGENTS TO SUBSTITUTED ISOPROPYLIDENE METHYLENEMALONATES

Haslego, Mark L.,Smith, Francis X.

, p. 421 - 428 (2007/10/02)

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