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(E)-3-[4-(2-Methyl-1-propenyl)phenyl]2-propenoic acid, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145589-32-8

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145589-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145589-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,5,8 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 145589-32:
(8*1)+(7*4)+(6*5)+(5*5)+(4*8)+(3*9)+(2*3)+(1*2)=158
158 % 10 = 8
So 145589-32-8 is a valid CAS Registry Number.

145589-32-8Downstream Products

145589-32-8Relevant academic research and scientific papers

A novel approach to the synthesis of benzoic and cinnamic acid derivatives with nor-isoprenoid substituents

Kryshtal, G. V.,Zhdankina, G. M.,Serebryakov, E. P.

, p. 866 - 869 (2007/10/02)

A novel strategy for the synthesis of 4-(nor-polyprenyl)-substituted benzoic acids and their esters of the general formula 1 as well as their vinylogs of the type 2, based on the use of terephthalic aldehyde (3) and its tetramethyl acetal (13), is elaborated.The carbonyl groups in dialdehydes 3 and 12 can be selectively involved in the reaction sequences leading to the introduction of both aliphatic and functional substituents in positions 1 and 4 of the benzene ring.

Bisphosphonate squalene synthetase inhibitors and method

-

, (2008/06/13)

Compounds which are inhibitors of cholesterol biosynthesis (by inhibiting de novo squalene biosynthesis), and thus are useful as hypocholesterolemic agents and antiatherosclerotic agents are provided which have the structure STR1 and analogs thereof, wherein R1, R2, R3 and R4 are the same or different and are H, lower alkyl, a metal ion or a prodrug ester; R5 is H, halogen or lower alkyl; Zq is substituted alkenyl, substituted alkynyl, mixed alkenyl-alkynyl or substituted phenylalkyl or, phenylalkenyl or phenylalkynyl, or alkyl, including all stereoisomers thereof. New methods for using such compounds to inhibit cholesterol biosynthesis are also provided.

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