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2(3H)-Furanone, dihydro-3-methylene-5,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29043-99-0

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29043-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29043-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,4 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29043-99:
(7*2)+(6*9)+(5*0)+(4*4)+(3*3)+(2*9)+(1*9)=120
120 % 10 = 0
So 29043-99-0 is a valid CAS Registry Number.

29043-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylidene-5,5-diphenyloxolan-2-one

1.2 Other means of identification

Product number -
Other names 3-Methylen-5,5-diphenyltetrahydrofuran-2-on

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:29043-99-0 SDS

29043-99-0Downstream Products

29043-99-0Relevant academic research and scientific papers

α-Methylene-γ-butyrolactones with molluscicidal activity

Rucker,Hostettmann,Gajewski,Lobbert,Boken

, p. 941 - 945 (2007/10/02)

The α-methylene-γ-butyrolactones 1-28 were tested in vitro for molluscicidal activity against Biomphalaria glabrata. The racemic compound 25 shows the best activity. The synthesis was carried out by modified Reformatzky reaction of the corresponding carbo

Electrogenerated Zinc as the Catalyst in the Allylation of Carbonyl Compounds. Direct Synthesis of α-Methylene-γ-Lactones

Rollin, Y.,Derien, S.,Dunach, E.,Gebehenne, C.,Perichon, J.

, p. 7723 - 7732 (2007/10/02)

The electroreduction of a catalytic amount of ZnBr2 in acetonitrile provided a active Zn*, able to catalyze the reductive coupling of allyl bromides and chlorides with carbonyl compounds with high regioselectivity.Substituted α-methylene γ-lactones were o

Dimetalation of N-tert-Butylmethacrylamide: A New Synthetic Reagent

Fitt, John J.,Gschwend, Heinz W.

, p. 4257 - 4259 (2007/10/02)

Dimetalation of N-tert-butylmethacrylamide with n-butyllithium gives a reagent equivalent to the dianion of methacrylic acid.Its reaction with various electrophiles and the transformation of certain primary products to α-methylene lactones is exemplified.

Synthesis of α-Methylene-γ-butyrolactones: A Structure-Activity Relationship Study of Their Allergenic Power

Schlewer, Gilbert,Stampf, Jean-Luc,Benezra, Claude

, p. 1031 - 1038 (2007/10/02)

Thirty-five α-methylene-γ-butyrolactones has been prepared and their allergenic properties tested on the skin of guinea pigs experimentally sensitized to (a) alantolactone (1), (b) isoalantolactone (2), and (c) α-methylene-γ-butyrolactone (3).The two firs

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