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88301-96-6

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88301-96-6 Usage

General Description

2-AMINO-3-(METHYLTHIOMETHYL)BENZOTRIFLUORIDE is a chemical compound with the molecular formula C9H10F3NS. It is a benzotriazole derivative with a methylthiomethyl group attached to the amino group. 2-AMINO-3-(METHYLTHIOMETHYL)BENZOTRIFLUORIDE is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also known for its ability to inhibit corrosion on metal surfaces and is used in the formulation of corrosion inhibitors. Additionally, 2-AMINO-3-(METHYLTHIOMETHYL)BENZOTRIFLUORIDE has potential applications in the field of organic synthesis due to its unique structure and reactivity. Overall, this chemical compound has diverse uses in various industries and research fields.

Check Digit Verification of cas no

The CAS Registry Mumber 88301-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,0 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88301-96:
(7*8)+(6*8)+(5*3)+(4*0)+(3*1)+(2*9)+(1*6)=146
146 % 10 = 6
So 88301-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H10F3NS/c1-14-5-6-3-2-4-7(8(6)13)9(10,11)12/h2-4H,5,13H2,1H3

88301-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methylsulfanylmethyl)-6-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names 2-methylthiomethyl-6-trifluoromethyl aniline

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:88301-96-6 SDS

88301-96-6Relevant articles and documents

Synthesis, sciatic nerve block activity evaluation and molecular docking of fluoro-substituted lidocaine analogs as local anesthetic agents

Li, Wen,Yan, Ying,Chang, Yingjie,Ding, Lina,Liu, Hongmin,You, Qidong

, p. 1783 - 1795 (2019/08/12)

Thirty fluoro-substituted lidocaine analogs (10a–e, 11a–e, 14a–e, 15a–e, 18a–e and 19a–e) were synthesized, and their sciatic nerve block activity were evaluated as local anesthesia. Most of the compounds displayed significant potency, and compound 10a in particular was much more potent than the parent lidocaine. Fifteen analogs including 10a demonstrated pKa values of 7.5–7.8 suitable for local anesthesia. Compound 10a, 14e, and lidocaine were docked into three target receptors of local anesthetics by molecular docking studies to delineate structure-activity relationships and explain the differences in activities. Hydrophobic interactions and hydrogen bonds were identified key to molecular binding, suggesting that optimization of these interactions and/or trifluoro-substitution at the benzene ring of lidocaine could enhance the properties of lidocine analogs for local anesthesia.

Substituted 2-alkylsulfonylalkyl nitrobenzenes and process for their preparation

-

, (2008/06/13)

The disclosure herein relates to substituted 2-alkylsulfonylalkyl nitrobenzenes and a process for the preparation thereof. The compounds herein are useful as intermediates in the preparation of certain substituted anilines used as reactants in the prepara

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