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1(2H)-Naphthalenone, 4-(3-chlorophenyl)-3,4-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82101-37-9

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82101-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82101-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,0 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82101-37:
(7*8)+(6*2)+(5*1)+(4*0)+(3*1)+(2*3)+(1*7)=89
89 % 10 = 9
So 82101-37-9 is a valid CAS Registry Number.

82101-37-9Downstream Products

82101-37-9Relevant academic research and scientific papers

A sertraline hydrochloride impurity preparation method (by machine translation)

-

, (2019/06/08)

The invention discloses a sertraline hydrochloride preparation method of impurities, in particular comprising a formula 6 by the Leuckart reaction to obtain a compound of the formula 7 compound, with the insulated hydrochloride salt obtained in the reaction formula 8 cis-isomer of the compound, wherein the formula 6 compound in the location of the chloropropyl substituted cyclohexanone substituted meta or para position. Preparation method of this invention is simple, high purity, obtained impurity can be used for qualitative and quantitative analysis, so as to improve the safety of medicine sertraline hydrochloride. (by machine translation)

5-Phenyl-3-ureidobenzazepin-2-ones as cholecystokinin-B receptor antagonists

Lowe III,Hageman,Drozda,McLean,Bryce,Crawford,Zorn,Morrone,Bordner

, p. 3789 - 3811 (2007/10/02)

A series of 5-phenyl-3-ureidobenzazepin-2-one cholecystokinin-B (CCK-B) receptor antagonists was synthesized using Beckmann ring expansion of a suitable 4-phenyl-1-tetralone as a key step. Structure-activity relationship studies revealed the importance of

REACTION OF PHENOLS AND THEIR DERIVATIVES WITH AROMATIC COMPOUNDS IN THE PRESENCE AF ACIDIC AGENTS. CONDENSATION OF 1-NAPHTHOL WITH MONOSUBSTITUTED DERIVATIVES OF BENZENE

Repinskaya, I. B.,Koryabkina, N. A.,Makarova, Z. S.,Koptyug, V. A.

, p. 754 - 760 (2007/10/02)

The isomeric composition and the relative formation rates of 4-(X-phenyl)-1-tetralones in the condensation of 1-naphthol with C6H5X (X=CH3, F, Cl, H) in the presence of aluminum bromide were determined.The obtained date demonstrate the electrophilic character of the particle which is formed from 1-naphthol and subsequently enters into reaction with benzene or its derivatives.The character of electrophilic activation of the phenols and their ethers in condensation reactions of this type is discussed.

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