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5-(METHYLTHIO)-2-NITROBENZOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 68701-32-6 Structure
  • Basic information

    1. Product Name: 5-(METHYLTHIO)-2-NITROBENZOIC ACID
    2. Synonyms: 5-(methylthio)-2-nitrobenzoic acid
    3. CAS NO:68701-32-6
    4. Molecular Formula: C8H7NO4S
    5. Molecular Weight: 213.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 68701-32-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 407.337°C at 760 mmHg
    3. Flash Point: 200.151°C
    4. Appearance: /
    5. Density: 1.489g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.642
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-(METHYLTHIO)-2-NITROBENZOIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-(METHYLTHIO)-2-NITROBENZOIC ACID(68701-32-6)
    12. EPA Substance Registry System: 5-(METHYLTHIO)-2-NITROBENZOIC ACID(68701-32-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 68701-32-6(Hazardous Substances Data)

68701-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68701-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,7,0 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68701-32:
(7*6)+(6*8)+(5*7)+(4*0)+(3*1)+(2*3)+(1*2)=136
136 % 10 = 6
So 68701-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO4S/c1-14-5-2-3-7(9(12)13)6(4-5)8(10)11/h2-4H,1H3,(H,10,11)

68701-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methylsulfanyl-2-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 5-methylthio-2-nitrobenzoic 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:68701-32-6 SDS

68701-32-6Relevant articles and documents

A highly selective fluorogenic substrate for imaging glutathione S-transferase P1: Development and cellular applicability in epigenetic studies

Mori, Masaya,Fujikawa, Yuuta,Kikkawa, Manami,Shino, Moeho,Sawane, Mei,Sato, Shiho,Inoue, Hideshi

supporting information, p. 8122 - 8125 (2019/07/15)

Pi-class glutathione S-transferase (GSTP1) is a molecular marker enzyme whose expression level is altered in various malignant tumour tissues. Herein, we report the first highly selective fluorogenic GSTP1 substrate, Ps-TG, and its membrane-permeable deri

Design, synthesis and insecticidal activities of novel anthranilic diamides containing fluorinated groups as potential ryanodine receptors activitors

Wu, Chang-Chun,Wang, Bao-Lei,Liu, Jing-Bo,Wei, Wei,Li, Yu-Xin,Liu, Yang,Chen, Ming-Gui,Xiong, Li-Xia,Yang, Na,Li, Zheng-Ming

supporting information, p. 1248 - 1251 (2017/06/19)

In order to search for novel potent and environmentally benign insecticides, a series of anthranilic diamides containing various fluorinated groups were designed and synthesized. Their structures were confirmed by 1H NMR, 13C NMR, s

Compositions and Methods for the Inhibition of Methyltransferases

-

Paragraph 0193, (2015/03/04)

Methods and compositions disclosed herein relate to detecting, analyzing, isolating and inhibiting methyltransferases, methyltransferase substrates, S-adenosyl-methionine-binding proteins and RNA, including for the treatment of disease.

POTENT SMALL MOLECULE INHIBITORS OF AUTOPHAGY, AND METHODS OF USE THEREOF

-

Page/Page column 104, (2014/09/29)

Certain aspects of the invention relate to small molecule autophagy inhibitors, and their use for treatment and prevention of cancers and acute pancreatitis. Medicinal chemistry studies led to small molecular autophagy inhibitors with improved potency and selectivity.

Novel phenylalanine derivatives

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Page/Page column 32, (2010/02/14)

Specific phenylalanine derivatives and analogues thereof have an antagonistic activity to α4 integrin. They are used as therapeutic agents for various diseases concerning α4 integrin.

Piperidyindoles as serotonin receptor ligands

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Page 9, (2010/02/05)

A pharmaceutical compound of the formula (I) in which R1 and R2 are each hydrogen or C1-6 alkyl, R3 is —SR10, —SOR10, —SO2R10, —COR10, —CH2OH or —CONHR11, where R10 is C1-6 alkyl and R11 is hydrogen or C1-6 alkyl, R4, R5, R6 and R7 are each hydrogen or C1-6 alkyl, provided that at least one of R4, R5, R6 and R7 is C1-6 alkyl, R8 and R9 are each hydrogen, halo, C1-6 alkyl or cyano, n is 0 or 1 and m is 2 or 3, x is a (a) or (b), and y is (c) or (d), wherein R12 and R13 are each hydrogen, C1- alkyl, cyclopropyl or cyclopropyl-C1-6 alkyl; and salts thereof.

Synthesis and antinephritic activities of quinoline-3-carboxamides and related compounds

Tsuji, Kiyoshi,Spears, Glen W.,Nakamura, Katsuya,Tojo, Takashi,Seki, Nobuo,Sugiyama, Aiko,Matsuo, Masaaki

, p. 85 - 88 (2007/10/03)

A series of linomide-related quinoline-3-carboxamides and their analogues was prepared and evaluated for antinephritic activities. The 6-MeS derivative 7a was highly effective in two nephritis models, namely chronic graft-versus-host disease and autoimmune MRL/l mice.

Reactions of 2H-3,1-Benzoxazine-2,4-(1H)dione (Isatoic Anhydride) (1) with Anions of 1,4-Dihydro-5H-Pyrazol-5-ones: Synthesis of Pyrazoloquinazolin-9-ones

Sircar, Jagadish C.,Capiris, Thomas,Kesten, Stephen J.

, p. 117 - 121 (2007/10/02)

Reactions of 2H-3,1-benzoxazine-2,4-(1H)dione (isatoic anhydride) (1) with anions of 1,4-dihydro-5H-pyrazol-5-ones (2) gave pyrazoloquinazolin-9-ones (3) via the nucleophilic attack of the anion 2b rather than 2a.However, in the case of 5-methoxyis

Pyrazolo[5,1-b]quinazolin-9-(4H)-ones and anti-allergic pharmaceutical compositions containing them

-

, (2008/06/13)

Certain pyrazolo[5,1-b]quinazolin-9-(4H)-ones are disclosed. These compounds prevent the allergic response in mammals. Novel alkylthioanthranilic acids, useful as intermediates, are also disclosed.

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