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Ethyl (2Z)-2-methylpenta-2,4-dienoate, also known as ethyl geranate, is a colorless liquid organic compound with the chemical formula C8H12O2. It is a derivative of pentadienoic acid, featuring a conjugated diene system with a methyl group at the 2-position and an ester group at the end of the carbon chain. ethyl (2Z)-2-methylpenta-2,4-dienoate is widely used in the flavor and fragrance industry due to its strong citrus-like aroma, resembling lemon and orange. Ethyl (2Z)-2-methylpenta-2,4-dienoate is synthesized through various methods, including the esterification of (2Z)-2-methylpenta-2,4-dienoic acid with ethanol. It is also found in natural sources such as citrus fruits and is used as a flavoring agent in food and beverages, as well as in the production of perfumes and cosmetics.

1572-72-1

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1572-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1572-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1572-72:
(6*1)+(5*5)+(4*7)+(3*2)+(2*7)+(1*2)=81
81 % 10 = 1
So 1572-72-1 is a valid CAS Registry Number.

1572-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (2Z)-2-methylpenta-2,4-dienoate

1.2 Other means of identification

Product number -
Other names ethyl 2-methyl-2,4-pentadienoate

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:1572-72-1 SDS

1572-72-1Downstream Products

1572-72-1Relevant articles and documents

A concise approach for the total synthesis of pseudolaric acid A

Xu, Tao,Li, Chuang-Chuang,Yang, Zhen

, p. 2630 - 2633 (2011)

A new strategy for the stereoselective total synthesis of natural product pseudolaric acid A (1) was accomplished in 16 steps from commercially available starting material, featuring a samarium diiodide (SmI2)-mediated intramolecular alkene-ketyl radical cyclization and a ring-closing metathesis (RCM) reaction to stereoselectively cast the unusual trans-fused [5-7]-bicyclic core of pseudolaric acid A (1).

Palladium-Promoted Neutral 1,4-Brook Rearrangement/Intramolecular Allylic Cyclization Cascade Reaction: A Strategy for the Construction of Vinyl Cyclobutanols

Zhang, Hao,Ma, Shiqiang,Yuan, Ziyun,Chen, Peng,Xie, Xingang,Wang, Xiaolei,She, Xuegong

, p. 3478 - 3481 (2017)

A cascade reaction to build vinyl cyclobutanol rings through activation of vinyl epoxides by palladium, followed by 1,4-Brook rearrangement and intramolecular cyclization with a palladium complex of the resulting carbon anion, is described. Through this cascade reaction, several highly substituted cyclobutanol substrates were achieved in good yields with high stereoselectivities.

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