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CAS

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33795-08-3

2,2-dimethyl-1-phenyl-cyclopropanecarboxylic acid is a cyclopropane derivative with a molecular formula C13H14O2. It features a cyclopropane ring to which a phenyl group is attached, and it is classified as a carboxylic acid due to the presence of a carboxyl group. This functional group, composed of a carbonyl and a hydroxyl group, endows the compound with unique chemical properties and reactivity, making it a valuable intermediate in chemical processes and the pharmaceutical industry.

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  • 33795-08-3 Structure

  • Basic information

    1. Product Name: 2,2-dimethyl-1-phenyl-cyclopropanecarboxylic acid
    2. Synonyms:
    3. CAS NO:33795-08-3
    4. Molecular Formula: C12H14O2
    5. Molecular Weight: 190.2384
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33795-08-3.mol
    9. Article Data: 0

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 309.6°C at 760 mmHg
    3. Flash Point: 145.8°C
    4. Appearance: N/A
    5. Density: 1.142g/cm3
    6. Vapor Pressure: 0.000272mmHg at 25°C
    7. Refractive Index: 1.557
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,2-dimethyl-1-phenyl-cyclopropanecarboxylic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,2-dimethyl-1-phenyl-cyclopropanecarboxylic acid(33795-08-3)
    12. EPA Substance Registry System: 2,2-dimethyl-1-phenyl-cyclopropanecarboxylic acid(33795-08-3)

  • 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: 33795-08-3(Hazardous Substances Data)

33795-08-3 Usage

Uses

Used in Organic Synthesis:
2,2-dimethyl-1-phenyl-cyclopropanecarboxylic acid is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure and reactivity allow for the formation of new molecules with potential applications in different fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2-dimethyl-1-phenyl-cyclopropanecarboxylic acid is utilized as an intermediate for the preparation of pharmaceuticals and biologically active compounds. Its cyclopropane ring and phenyl group provide a structural foundation that can be further modified to develop new drugs with specific therapeutic properties.
Used in Chemical Processes:
2,2-dimethyl-1-phenyl-cyclopropanecarboxylic acid is employed as an important intermediate in various chemical processes. Its chemical properties allow it to participate in a range of reactions, contributing to the synthesis of complex molecules and materials with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 33795-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,9 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33795-08:
(7*3)+(6*3)+(5*7)+(4*9)+(3*5)+(2*0)+(1*8)=133
133 % 10 = 3
So 33795-08-3 is a valid CAS Registry Number.

33795-08-3SDS

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 2,2-dimethyl-1-phenylcyclopropane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,2-DIFLUOROSUCCINIC 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:33795-08-3 SDS

33795-08-3Synthetic route

2-phenyl-acrylic acid methyl ester
1865-29-8

2-phenyl-acrylic acid methyl ester

diphenylisoporopylsulfonium iodide
74898-44-5

diphenylisoporopylsulfonium iodide

(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid
33795-08-3

(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid

Conditions
ConditionsYield
(i) LiN(iPr)2, (ii) /BRN= 1907525/, (iii) KOH, MeOH; Multistep reaction;
(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid
33795-08-3

(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid

(rac)-5-(4-fluorophenyl)-3,9-diazaspiro[5.5]undecan-2-one

(rac)-5-(4-fluorophenyl)-3,9-diazaspiro[5.5]undecan-2-one

9-{[2,2-dimethyl-1-phenylcyclopropyl]carbonyl}-5-(4-f luorophenyl)-3,9-diazaspiro[5.5]undecan2-one

9-{[2,2-dimethyl-1-phenylcyclopropyl]carbonyl}-5-(4-f luorophenyl)-3,9-diazaspiro[5.5]undecan2-one

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃;73%
diazomethane
186581-53-3, 908094-01-9

diazomethane

(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid
33795-08-3

(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid

(1-Phenyl-2,2-dimethylcyclopropyl)-essigsaeuremethylester
33795-09-4

(1-Phenyl-2,2-dimethylcyclopropyl)-essigsaeuremethylester

Conditions
ConditionsYield
Multistep reaction;
(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid
33795-08-3

(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid

1,1-Diphenyl-2-(1-phenyl-2,2-dimethylcyclopropyl)-ethanol
33795-10-7

1,1-Diphenyl-2-(1-phenyl-2,2-dimethylcyclopropyl)-ethanol

(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid
33795-08-3

(rac)-2,2-dimethyl-1-phenylcyclopropanecarboxylic acid

1-(2,2-Diphenylvinyl)-1-phenyl-2,2-dimethyl-cyclopropan
33795-11-8

1-(2,2-Diphenylvinyl)-1-phenyl-2,2-dimethyl-cyclopropan

Conditions
ConditionsYield
Multi-step reaction with 3 steps
3: TsOH, phthalic anhydride
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