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CAS

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14034-95-8

2,5-ditert-butylbenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14034-95-8 Structure

  • Basic information

    1. Product Name: 2,5-ditert-butylbenzoic acid
    2. Synonyms: 2,5-ditert-butylbenzoic acid
    3. CAS NO:14034-95-8
    4. Molecular Formula: C15H22O2
    5. Molecular Weight: 234.33398
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14034-95-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,5-ditert-butylbenzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-ditert-butylbenzoic acid(14034-95-8)
    11. EPA Substance Registry System: 2,5-ditert-butylbenzoic acid(14034-95-8)

  • 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: 14034-95-8(Hazardous Substances Data)

14034-95-8 Usage

Molecular weight

234.33 g/mol

Appearance

White crystalline solid

Melting point

162-164°C

Solubility

Sparingly soluble in water

Functional groups

Benzoic acid, two tert-butyl groups

Use as a stabilizer

Prevents degradation of polymers (e.g. polyvinyl chloride) from heat and UV radiation

Use as a chemical intermediate

In the synthesis of various pharmaceuticals and agrochemicals

Potential applications

Organic electronics, corrosion inhibition in metal surfaces

Check Digit Verification of cas no

The CAS Registry Mumber 14034-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,3 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14034-95:
(7*1)+(6*4)+(5*0)+(4*3)+(3*4)+(2*9)+(1*5)=78
78 % 10 = 8
So 14034-95-8 is a valid CAS Registry Number.

14034-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-ditert-butylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2,5-Di-tert.-butyl-benzoesaeure

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:14034-95-8 SDS

14034-95-8Relevant articles and documents

The rate retarding effect of alkyl groups on arene metalation quantified

Baston, Eckhard,Wang, Qian,Schlosser, Manfred

, p. 667 - 670 (2000)

Metalation/trapping sequences applied to relatively inert, tert-alkyl substituted arenes tend to give poor yields unless the reagent is used in high concentrations. Under optimized conditions, even 1,4-bis(tert- butyl)benzene, 1,1,3,3-tetramethylindane an

Efficient chemoselective carboxylation of aromatics to arylcarboxylic acids with a superelectrophilically activated carbon dioxide-Al2Cl6/Al system

Olah, George A.,Toeroek, Bela,Joschek, Jens P.,Bucsi, Imre,Esteves, Pierre M.,Rasul, Golam,Prakash, G. K. Surya

, p. 11379 - 11391 (2007/10/03)

Aromatic carboxylic acids are obtained in good to excellent yield essentially free of diaryl ketones by carboxylation of aromatics with a carbon dioxide-Al2Cl6/Al system at moderate temperatures (20-80°C). To optimize reaction condit

Dimetalation: The acidity of monometalated arenes towards superbasic reagents

Baston, Eckhard,Maggi, Raimondo,Friedrich, Kirstin,Schlosser, Manfred

, p. 3985 - 3989 (2007/10/03)

Twofold hydrogen/metal interconversions ("dimetalations") can be accomplished with "spiny" arenes (tert-butylbenzene, 1,4-di-tert-butylbenzene, 1,1,3,3-tetramethylindane and congeners) and N,N-crowded anilines (2,2,6,6-tetramethyl-1-phenylpiperidine and N

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