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Benzoic acid, 2-[2-(4-methylphenyl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86693-59-6

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86693-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86693-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,9 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86693-59:
(7*8)+(6*6)+(5*6)+(4*9)+(3*3)+(2*5)+(1*9)=186
186 % 10 = 6
So 86693-59-6 is a valid CAS Registry Number.

86693-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(4-methylphenyl)ethyl]benzoic acid

1.2 Other means of identification

Product number -
Other names 2-(2-(4-methylphenyl)ethyl) benzoic acid

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:86693-59-6 SDS

86693-59-6Downstream Products

86693-59-6Relevant academic research and scientific papers

Highly linear selective cobalt-catalyzed addition of aryl imines to styrenes: Reversing intrinsic regioselectivity by ligand elaboration

Xu, Wengang,Yoshikai, Naohiko

supporting information, p. 14166 - 14170 (2015/02/19)

Highly linear selective, imine-directed hydroarylation of styrene has been achieved with cobalt-based catalytic systems featuring bis(2,4-dimethoxyphenyl)(phenyl)phosphine and either 2-methoxypyridine or DBU as a ligand and a Lewis base additive, respectively, thus affording a variety of 1,2-diarylethanes (bibenzyls) in good yields under mild reaction conditions. The triarylphosphine controls the regioselectivity, while the Lewis base significantly accelerates the reaction. Ligand screening and deuterium-labeling studies provide implications about the roles of the ligand and the Lewis base in the crucial C-C reductive elimination step.

4-Aminoquinolines: Novel nociceptin antagonists with analgesic activity

Shinkai,Ito,Iida,Kitao,Yamada,Uchida

, p. 4667 - 4677 (2007/10/03)

Small-molecule nociceptin antagonists were synthesized to examine their therapeutic potential. After a 4-aminoquinoline derivative was found to bind with the human ORL1 receptor, a series of 4-aminoquinolines and related compounds were synthesized and their binding was evaluated. Elucidation of structure - Activity relationships eventually led to the optimum compounds. One of these compounds, N-(4-amino-2-methylquinolin-6-yl)-2-(4-ethylphenoxymethyl)benzamide hydrochloride (11) not only antagonized nociceptin-induced allodynia in mice but also showed analgesic effect in a hot plate test using mice and in a formalin test using rats. Its analgesic effect was not antagonized by the opioid antagonist naloxone. These results indicate that this nociceptin antagonist has the potential to become a novel type of analgesic that differs from μ-opioid agonists.

Substituted dibenzocycloheptenimines

-

, (2008/06/13)

The present invention provides a compound of formula (I): STR1 or a pharmaceutically acceptable salt thereof, wherein one of R1, R2, R3 and R4 represents a hydrocarbon or hydrocarbyloxycarbonyl group and the rem

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