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4-phenyl-1,2-cyclohexanedicarboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1444-93-5

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1444-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1444-93-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1444-93:
(6*1)+(5*4)+(4*4)+(3*4)+(2*9)+(1*3)=75
75 % 10 = 5
So 1444-93-5 is a valid CAS Registry Number.

1444-93-5Relevant academic research and scientific papers

Simple and efficient synthesis of new tricarboxylic acids bearing cyclohexane and norbornane fragments

Firstova,Kofanov,Krasovskaya,Danilova

, p. 867 - 869 (2017)

A synthesis new aryl alicyclic tricarboxylic acids bearing two carboxyl groups at either cyclohexane or norbornane fragment and one carboxyl group at the benzene ring was devel-oped. Tricarboxylic acids of this type are promising monomers for the synthesis of hetero-cyclic polymers.

Practical synthesis of four different pseudoenantiomeric organocatalysts with both cis- and trans-substituted 1,2-cis-cyclohexanediamine structures from a common intermediate

Lee, Hyo-Jun,Arumugam, Natarajan,Almansour, Abdulrahman I.,Kumar, Raju Suresh,Maruoka, Keiji

, p. 5263 - 5269 (2018/05/29)

A new and convenient approach has been deviced for the practical synthesis of structurally robust, four different pseudoenantiomeric amino Tf-amido organocatalysts with the unique cis- and trans-substituted 1,2-cis-cyclohexanediamine structures. These pse

Saturated heterocycle-condensed diphenylisoindolones: Fused-skeleton tetrahydro-1,3-oxazines, oxazolidines and imidazolidines

Sohar, Pal,Stajer, Geza,Szabo, Angela E.,Bernath, Gabor

, p. 187 - 195 (2007/10/03)

The addition of benzene to cis-4-cyclohexene-1,2-dicarboxylic anhydride yielded c-2-benzoyl-t-5-phenyl-r-1-cyclohexanecarboxylic acid (72%), or in another reaction, the 4-phenyl isomer (67%). With bifunctional reagents, saturated tricyclic or partially sa

FUSED-SKELETON SATURATED SIX-MEMBERED 1,3-N,O, N,N AND N,S HETEROCYCLES, FUSED-SKELETON ARYL-SUBSTITUTED SATURATED ISOINDOLONES

Bernath, G.

, p. 509 - 530 (2007/10/02)

In the introduction, a brief survey is given of the main types of fused-skeleton saturated six-membered 1,3-heterocycles serving as model compounds in our earlier investigations and as starting compounds in the present studies.The synthesis and conformational analysis of aryl-substituted fused-skeleton saturated 1,3-oxazines and of aryl-substituted hetero-condensed saturated isoindolones are treated. cis-trans isomerization in the saturated isoindolone moiety of the resulting tricyclic, tetracyclic and pentacyclic systems is discussed in connection with the ring-closure reactions of cis- and trans-1,2-disubstituted 1,2- and 1,3-difunctional alicyclic compounds to give alicycle-fused six-membered 1,3-heterocycles.The cycloaddition reactions of dihydro-1,3 and 3,1-oxazines and the conformations of the alicycle-fused tetrahydrooxazine-azetidinone derivatives obtained are presented.Methods are given for the preparation of saturated thiazolo- and thiazinoquinazolinones.Unambiguous, mainly one-pot syntheses for the preparation of 1,3-heterocycles by a retro Diels-Alder method are discussed.

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