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2-Butenal, 2-methyl-4-phenoxy-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62285-79-4

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62285-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62285-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,8 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62285-79:
(7*6)+(6*2)+(5*2)+(4*8)+(3*5)+(2*7)+(1*9)=134
134 % 10 = 4
So 62285-79-4 is a valid CAS Registry Number.

62285-79-4SDS

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-methyl-4-phenoxybut-2-enal

1.2 Other means of identification

Product number -
Other names (E)-4-Phenoxy-2-methyl-2-butenal

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:62285-79-4 SDS

62285-79-4Relevant academic research and scientific papers

Synthesis and vitamin D receptor affinity of 16-oxa vitamin D3 analogues

Ibe, Kouta,Yamada, Takeshi,Okamoto, Sentaro

, p. 10188 - 10200 (2019/12/25)

Two novel 16-oxa-vitamin D3 analogues were synthesized using a tandem Ti(ii)-mediated enyne cyclization/Cu-catalyzed allylation, Ru-catalyzed ring-closing metathesis reaction, and a low-valent titanium (LVT)-mediated stereoselective radical red

Regio- and Stereo-selective Oxidation of gem-Dimethyl Olefins via -Sigmatropic Rearrangement of Allyl Amine Oxides

Inoue, Seiichi,Iwase, Norimichi,Miyamoto, Osamu,Sato, Kikumasa

, p. 2035 - 2038 (2007/10/02)

Highly regio- and stereo-selective oxidation sequences are described for the efficient conversion of the gem-dimethyl olefin terminus of acyclic terpenes to terminal trans-allylic alcohols and trans α,β-unsaturated aldehydes.

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