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3-Buten-2-one, 1,1-dimethoxy-4-phenyl-, (3E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76504-50-2

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76504-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76504-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,0 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76504-50:
(7*7)+(6*6)+(5*5)+(4*0)+(3*4)+(2*5)+(1*0)=132
132 % 10 = 2
So 76504-50-2 is a valid CAS Registry Number.

76504-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1,1-dimethoxy-4-phenyl-3-buten-2-one

1.2 Other means of identification

Product number -
Other names (E)-1,1-Dimethoxy-4-phenyl-but-3-en-2-one

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:76504-50-2 SDS

76504-50-2Downstream Products

76504-50-2Relevant academic research and scientific papers

Preparation of 3-fluoro-5-hydroxy-4--2(5H)-furanone

Komatsu, Yuzo,Kitazume, Tomoya

, p. 101 - 104 (1998)

Synthesis of 3-fluoro-5-hydroxy-4--2(5H)-furanone as an inhibitor of the phospholipase A2 (PLA2) was described. - Keywords: Bioactive materials; Inhibitor

Synthesis and Spectral Characterization of γ-Hydroxy-Δα,β-butenolides Possessing a Conjugated Substituent at the β-Position

Ito, Masayoshi,Iwata, Tsutomu,Tsukida, Kiyoshi

, p. 4346 - 4351 (2007/10/02)

Conjugated γ-hydroxybutenolides (6a-h, 10, and 11) were synthesized in three steps starting from various aldehydes (3a-h and 7), and their spectral characteristics were compared with those of unconjugated butenolides (12 and 13).Keywords-conjugated γ-hydr

OXYGEN TRANSFER DURING THE COPPER INDUCED REACTION OF α,β-EPOXY DIAZOMETHYL KETONES

Thijs, L.,Zwanenburg, B.

, p. 2145 - 2148 (2007/10/02)

Reactions of α,β-epoxy diazomethyl ketones 1a-i with activated copper powder or copper(II) sulfate in methanol (or ethanol) lead to 1,1-dialkoxy-but-3-ene-2-ones 2 (or 3) in good yields.This process of oxygen transfer proceeds via initially generated keto-carbenoids which react intramolecularly with the epoxide function to give bicyclic intermediates 10.Release of strain and subsequent ring opening produces but-2-ene-1,2-diones which acetalise to give the ultimate reaction products 2 (or 3).With copper as catalyst byproducts were isolated viz 1,1-dialkoxy-4-hydroxy-butane-2-ones (4 and 5), and indanone derivate 6.An explanation for these side reactions has been given.

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