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2-Naphthaleneethanol, 4-methylbenzenesulfonate is a complex organic chemical compound with the molecular formula C18H18O3S. It is a derivative of 2-napthaleneethanol, where a 4-methylbenzenesulfonate group is attached to the molecule. 2-Naphthaleneethanol, 4-methylbenzenesulfonate is characterized by its unique structure, which combines the aromatic properties of naphthalene and benzene with the hydrophilic nature of the sulfonate group. It is typically synthesized through a series of chemical reactions and is used in various applications, such as in the production of pharmaceuticals, dyes, and other specialty chemicals. Due to its specific functional groups, it may exhibit unique chemical properties and reactivity, making it a valuable compound in organic synthesis and chemical research.

7175-35-1

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7175-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7175-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7175-35:
(6*7)+(5*1)+(4*7)+(3*5)+(2*3)+(1*5)=101
101 % 10 = 1
So 7175-35-1 is a valid CAS Registry Number.

7175-35-1Relevant academic research and scientific papers

Discovery of SMP-304, a novel benzylpiperidine derivative with serotonin transporter inhibitory activity and 5-HT1Aweak partial agonistic activity showing the antidepressant-like effect

Yoshinaga, Hidefumi,Masumoto, Shuji,Koyama, Koji,Kinomura, Naoya,Matsumoto, Yuji,Kato, Taro,Baba, Satoko,Matsumoto, Kenji,Horisawa, Tomoko,Oki, Hitomi,Yabuuchi, Kazuki,Kodo, Toru

, p. 293 - 304 (2016/12/22)

We report the discovery of a novel benzylpiperidine derivative with serotonin transporter (SERT) inhibitory activity and 5-HT1Areceptor weak partial agonistic activity showing the antidepressant-like effect. The 3-methoxyphenyl group and the ph

Stereoselective synthesis of enantiopure analogues of (-)-cephalotaxine

Berhal, Farouk,Perard-Viret, Joelle,Royer, Jacques

scheme or table, p. 325 - 332 (2010/06/12)

The asymmetric total synthesis of three analogues of (-)-cephalotaxine with structural modification of the aromatic ring was achieved in 16 steps and acceptable overall yields. The procedure used was quite similar to that reported by our group for the tot

Melanocortin receptor ligands

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Page/Page column 24, (2010/11/08)

Disclosed are MC-4 and/or MC-3 receptor ligands, the ligands having a structure according to Formula (I): wherein R2, R4, R4′, R5, R6, R6′, R7, R8, R8′, R9, R9′, R10, Ar, Z1, Z2, Z3, X, B, D, p, q, r and s are as described in the specification and claims, and optical isomers, diastereomers or enantiomers thereof; pharmaceutically-acceptable salts, hydrates, and biohydrolyzable esters, amides or imides thereof. Also disclosed are pharmaceutical compositions comprising the ligands of Formula (I), as well as methods of treating diseases mediate by the MC-4/MC-3 receptors, as described in the Detailed Descriptions section of the specification.

Pyridyl- and/or pyridoyl-(piperid-4-yl) ureas and analogues thereof

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, (2008/06/13)

The invention concerns the preparation of compounds of formula STR1 and acid addition and quaternary ammonium salts thereof, wherein the dotted line represents an optional bond, Ar represents a ring system of formula STR2 in which Q is O, S, --CR7/s

Piperid-4-yl ureas and thio ureas used as antidepressant agents

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, (2008/06/13)

The invention concerns the preparation of compounds of formula STR1 and acid addition and quaternary ammoniun salts thereof, wherein the dotted line represents an optional bond, Ar represents a ring system of formula STR2 in which Q is O, S, --CR7/s

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