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α-Isopropyl-4-methyl-γ-oxobenzolbutansaeure, also known as α-isopropylmalic acid, is a chemical compound with the molecular formula C11H14O4. It is a derivative of malic acid, featuring an isopropylmalic acid structure with an additional methyl group at the 4-position and an isopropylmalic acid side chain. This organic compound is characterized by its unique structure, which includes a γ-oxo group and a benzene ring. It is used in various applications, such as in the synthesis of pharmaceuticals and other organic compounds, due to its versatile chemical properties. The compound's specific structure allows it to participate in a range of chemical reactions, making it a valuable intermediate in organic synthesis.

78309-97-4

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78309-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78309-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,0 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78309-97:
(7*7)+(6*8)+(5*3)+(4*0)+(3*9)+(2*9)+(1*7)=164
164 % 10 = 4
So 78309-97-4 is a valid CAS Registry Number.

78309-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name α-Isopropyl-4-methyl-γ-oxobenzolbutansaeure

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

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More Details:78309-97-4 SDS

78309-97-4Relevant academic research and scientific papers

Naturally Occuring Terpene Derivatives. 322. Synthesis of Sesquiterpenes from Heterotheca Species

Bohlmann, Ferdinand,Mailahn, Wolfgang

, p. 1091 - 1098 (2007/10/02)

Seven sesquiterpenes (7a, b, 8, 18a, 20b, 21, 23) isolated from two Heterotheca species have been synthesized.While 7a, b and 8 with an anomalous carbon skeleton were prepared via the 2-isopropyltetralone 6, the synthesis of the four others, all being cad

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