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CAS

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61203-95-0

TRANS-1-BUTYL-4-PHENYLCYCLOHEXANE is a colorless liquid chemical compound belonging to the cyclohexane family, characterized by a molecular formula of C18H30 and a molar mass of 246.43 g/mol. It is primarily utilized as an intermediate in organic synthesis, allowing for the production of various organic compounds through chemical reactions. Additionally, it serves as a solvent in certain industrial processes. Due to potential health hazards, it requires careful handling and appropriate safety measures.

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  • 61203-95-0 Structure

  • Basic information

    1. Product Name: TRANS-1-BUTYL-4-PHENYLCYCLOHEXANE
    2. Synonyms: TRANS-1-BUTYL-4-PHENYLCYCLOHEXANE
    3. CAS NO:61203-95-0
    4. Molecular Formula: C16H24
    5. Molecular Weight: 216.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 61203-95-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 307°C at 760 mmHg
    3. Flash Point: 134.7°C
    4. Appearance: /
    5. Density: 0.896g/cm3
    6. Vapor Pressure: 0.00135mmHg at 25°C
    7. Refractive Index: 1.497
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: TRANS-1-BUTYL-4-PHENYLCYCLOHEXANE(CAS DataBase Reference)
    11. NIST Chemistry Reference: TRANS-1-BUTYL-4-PHENYLCYCLOHEXANE(61203-95-0)
    12. EPA Substance Registry System: TRANS-1-BUTYL-4-PHENYLCYCLOHEXANE(61203-95-0)

  • 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: 61203-95-0(Hazardous Substances Data)

61203-95-0 Usage

Uses

Used in Organic Synthesis:
TRANS-1-BUTYL-4-PHENYLCYCLOHEXANE is used as an intermediate in organic synthesis for the production of other organic compounds. Its versatile chemical structure allows it to undergo various reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Industrial Processes as a Solvent:
In certain industries, TRANS-1-BUTYL-4-PHENYLCYCLOHEXANE is employed as a solvent due to its ability to dissolve a wide range of substances. Its use in this capacity aids in various manufacturing processes, including the production of paints, coatings, and adhesives, as well as in the extraction and purification of certain compounds.
Used in Chemical Research:
TRANS-1-BUTYL-4-PHENYLCYCLOHEXANE is also utilized in chemical research as a model compound for studying the properties and reactions of cyclohexane derivatives. Its unique structure provides insights into the behavior of similar compounds and contributes to the development of new synthetic methods and applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 61203-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,0 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61203-95:
(7*6)+(6*1)+(5*2)+(4*0)+(3*3)+(2*9)+(1*5)=90
90 % 10 = 0
So 61203-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H24/c1-2-3-7-14-10-12-16(13-11-14)15-8-5-4-6-9-15/h4-6,8-9,14,16H,2-3,7,10-13H2,1H3/t14-,16-

61203-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-1-butyl-4-phenylcyclohexane

1.2 Other means of identification

Product number -
Other names 4-N-BUTYL CYCLOHEXYL BENZENE

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:61203-95-0 SDS

61203-95-0Relevant articles and documents

Synthesis of Mesogenic Compounds, Catalyzed by Metal Complexes. II. A New Method of Synthesis of 4,4'-Dialkylbiphenyls

Bumagin, N. A.,Luzikova, E. V.,Beletskaya, I. P.

, p. 1487 - 1491 (2007/10/03)

A new method for the synthesis of 4,4'-dialkylbiphenyls containing both n-alkyl- and 4-trans-n-alkylcyclohexyl substituents, based on highly selective reactions of monoalkylation and monoacylation of 1,4-dibromobenzene in the presence of palladium complexes is developed.

CONVENIENT SYNTHESIS OF 4-(TRANS-4 prime -N-ALKYLCYCLOHEXYL) BENZOIC ACIDS.

Szczucinski,Dabrowski

, p. 55 - 64 (2007/10/02)

A convenient method of obtaining 4-(trans-4 prime -n-alkylcyclohexyl) benzoic acids from alkanoyl chlorides, cyclohexane and benzene is described. Homologous series of above mentioned acids and their nitriles with alkyl tail 2 to 10 carbon atoms were prepared and temperatures of their phase transitions were determined.

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