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Benzaldehyde, 4-methoxy-3-(1-methylethoxy)-2-(1-methyl-2-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

188255-40-5

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188255-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188255-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,2,5 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 188255-40:
(8*1)+(7*8)+(6*8)+(5*2)+(4*5)+(3*5)+(2*4)+(1*0)=165
165 % 10 = 5
So 188255-40-5 is a valid CAS Registry Number.

188255-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-but-3-en-2-yl-4-methoxy-3-propan-2-yloxybenzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:188255-40-5 SDS

188255-40-5Relevant academic research and scientific papers

TBuO 2H/Cu(acac) 2-Mediated Intramolecular Oxidative Lactonization of o -Allyl Arylaldehydes: Synthesis of 1-Oxoisochromans

Chang, Meng-Yang,Lai, Kai-Xiang,Chen, Kuan-Ting

, p. 527 - 537 (2020/10/19)

A concise route for the tBuO 2H/Cu(acac) 2-mediated synthesis of 1-oxoisochromans is described. This includes: (i) oxidation of oxygenated o -allyl arylaldehydes and (ii) sequential intramolecular lactonization of the resulting olefin-containing benzoic acids. A plausible mechanism is proposed and discussed.

A novel method for the synthesis of substituted naphthalenes and phenanthrenes

De Koning, Charles B.,Michael, Joseph P.,Rousseau, Amanda L.

, p. 787 - 797 (2007/10/03)

A new method for the synthesis of substituted naphthalenes and phenanthrenes was discussed. A formal synthesis of tanshinone I was also studied. Natural products that contain a naphthalene or phenanthrene nucleus often exhibit biological activity, which makes them attractive targets in organic synthesis. The results showed that the reaction can be proceed through at least two different pathways.

A novel synthesis subtituted naphthalenes

De Koning, Charles B.,Michael, Joseph P.,Rousseau, Ainanda L.

, p. 893 - 896 (2007/10/03)

Irradiation of 2-allylated acylbenzenes in DMF in the presence of potassium tert-butoxice constitutes a novel synthesis of substituted naphthalenes, including arylnaphthalenes. Typical examples including the conversions (1) → (2), (8) → (11) and (15) → (16).

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