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4-[acetyl(methyl)amino]benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 26961-99-9 Structure
  • Basic information

    1. Product Name: 4-[acetyl(methyl)amino]benzoic acid
    2. Synonyms:
    3. CAS NO:26961-99-9
    4. Molecular Formula: C10H11NO3
    5. Molecular Weight: 193.1992
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26961-99-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 369.5°C at 760 mmHg
    3. Flash Point: 177.3°C
    4. Appearance: N/A
    5. Density: 1.257g/cm3
    6. Vapor Pressure: 4.11E-06mmHg at 25°C
    7. Refractive Index: 1.594
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-[acetyl(methyl)amino]benzoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-[acetyl(methyl)amino]benzoic acid(26961-99-9)
    12. EPA Substance Registry System: 4-[acetyl(methyl)amino]benzoic acid(26961-99-9)
  • 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: 26961-99-9(Hazardous Substances Data)

26961-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26961-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,6 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26961-99:
(7*2)+(6*6)+(5*9)+(4*6)+(3*1)+(2*9)+(1*9)=149
149 % 10 = 9
So 26961-99-9 is a valid CAS Registry Number.

26961-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[acetyl(methyl)amino]benzoic acid

1.2 Other means of identification

Product number -
Other names -

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:26961-99-9 SDS

26961-99-9Relevant articles and documents

Nickel-catalyzed carboxylation of aryl and vinyl chlorides employing carbon dioxide

Fujihara, Tetsuaki,Nogi, Keisuke,Xu, Tinghua,Terao, Jun,Tsuji, Yasushi

supporting information; experimental part, p. 9106 - 9109 (2012/07/13)

Nickel-catalyzed carboxylation of aryl and vinyl chlorides employing carbon dioxide has been developed. The reactions proceeded under a CO2 pressure of 1 atm at room temperature in the presence of nickel catalysts and Mn powder as a reducing agent. Various aryl chlorides could be converted to the corresponding carboxylic acid in good to high yields. Furthermore, vinyl chlorides were successfully carboxylated with CO2. Mechanistic study suggests that Ni(I) species is involved in the catalytic cycle.

Pyran-4-ylmethyl substituted arylalkylaryl-, arylalkenylylaryl-, and arylalkynylarylurea inhibitors of 5-lipoxygenase

-

, (2008/06/13)

Compounds of structure STR1 where W is selected from STR2 where Q is oxygen or sulfur, R5 and R6 are independently selected from hydrogen and alkyl, or R5 and R6, together with the nitrogen atoms to which they a

Heteroatom substituted propanyl derivatives having 5-lipoxygenase inhibitory activity

-

, (2008/06/13)

Compounds of the structure STR1 where R1 is alkyl of one to four carbon atoms and R2 is selected from (a) alkenyl of one to four carbon atoms, (b) STR2 (c) STR3 and (d) STR4 are potent inhibitors of lipoxygenase enzymes and thus inhibit the biosynthesis of leukotrienes. These compounds are useful in the treatment or amelioration of allergic and inflammatory disease states.

TRANS-1,4-DIALKOXYCYCLOHEXYL SUBSTITUTED ARYLALKYLARYL- ARYLALKENYLARYL-, AND ARYLALKYNYLARYLUREA INHIBITORS OF 5-LIPOXYGENASE

-

, (2008/06/13)

Compounds of stracture where W is selected from the group consisting of where Q is oxygen or sulfur, R7 and R8 are independently selected from hydrogen and alkyl, or R7 and R8, together with the nitrogen atoms to which they are attached, define a radical

((4-ALKOXYPYRAN-4-YL) SUBSTITUTED) ETHER, ARYLALKYL-, ARYLALKENYL-, AND ARYLALKYNYL)UREA INHIBITORS OF 5-LIPOXYGENASE

-

, (2008/06/13)

Compounds of the structure where W is selected from where Q is oxygen or sulfur, R6and R7 are hydrogen or alkyl, or R6 and R7 , together with the nitrogen atoms to which they are attached, define a radical of formula Z is -CH2-, oxygen, sulfur, or -NR9,

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