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2-Furanol, tetrahydro-3,4-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92541-00-9

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92541-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92541-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,4 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92541-00:
(7*9)+(6*2)+(5*5)+(4*4)+(3*1)+(2*0)+(1*0)=119
119 % 10 = 9
So 92541-00-9 is a valid CAS Registry Number.

92541-00-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-diphenyloxolan-2-ol

1.2 Other means of identification

Product number -
Other names 2-Furanol,tetrahydro-3,4-diphenyl

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:92541-00-9 SDS

92541-00-9Upstream product

92541-00-9Downstream Products

92541-00-9Relevant academic research and scientific papers

REACTIONS OF OXIRANES WITH ALKALI METALS: INTERMEDIACY OF RADICAL-ANIONS

Gurudutt, K. N.,Pasha, M. A.,Ravindranath, B.,Srinivas, P.

, p. 1629 - 1632 (1984)

Reaction of oxiranes with alkali metals in aprotic solvents yields a variety of products depending on the nature of the metal and the structure of the oxirane.Deoxygenation to olefins is the major reaction in case of lithium.Rearrangement to carbonyl compounds, reduction to alcohols and formation of dimeric products occur when oxiranes are treated with sodium.All the reactions could be rationalised by a mechanism involving an initial single electron transfer leading to the formation of radical-anion intermediate.

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