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39077-35-5

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39077-35-5 Usage

Furan class of organic compounds

characterized by a tetrahydrofuran ring

Diphenylmethylidene group attached

a group consisting of two phenyl rings attached to a methylidene group

Colorless to pale yellow liquid

appearance of the compound

Molecular weight

284.372 g/mol

Use in organic synthesis

serves as a reagent in various chemical reactions

Unique structure and properties

makes it useful in the development of new pharmaceuticals and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 39077-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,7 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39077-35:
(7*3)+(6*9)+(5*0)+(4*7)+(3*7)+(2*3)+(1*5)=135
135 % 10 = 5
So 39077-35-5 is a valid CAS Registry Number.

39077-35-5SDS

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-benzhydrylideneoxolane

1.2 Other means of identification

Product number -
Other names 2-(diphenylmethylidene)tetrahydrofuran

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:39077-35-5 SDS

39077-35-5Relevant articles and documents

Cu(I)-catalyzed cascade reaction of N-tosylhydrazones with 3-butyn-1-ol: A new synthesis of tetrahydrofurans

Hossain, Mohammad Lokman,Wang, Kang,Ye, Fei,Zhang, Yan,Wang, Jianbo

, p. 115 - 122 (2017)

The Cu(I)-catalyzed cascade coupling/cyclization reaction of N-tosylhydrazones with 3-butyn-1-ol has been explored. This new strategy represents a simple platform for the synthesis of tetrahydrofurans in moderate to good yields.

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