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Trans-3-Methylcyclobutanecarboxylic acid, also known as trans-3-Methylcyclobutane-carboxylic acid, is a carboxylic acid compound with the molecular formula C6H10O2. It is a colorless liquid with a fruity odor and is often used as an intermediate in the synthesis of various organic compounds.

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  • 87863-09-0 Structure
  • Basic information

    1. Product Name: trans-3-Methylcyclobutanecarboxylic acid
    2. Synonyms: trans-3-Methylcyclobutanecarboxylic acid;(1s,3r)-3-Methylcyclobutane-1-carboxylic acid;trans-3-Methylcyclobutanecarboxylic acid - M10527
    3. CAS NO:87863-09-0
    4. Molecular Formula: C6H10O2
    5. Molecular Weight: 114.143
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87863-09-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 194.0±8.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.105±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.81±0.40(Predicted)
    10. CAS DataBase Reference: trans-3-Methylcyclobutanecarboxylic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: trans-3-Methylcyclobutanecarboxylic acid(87863-09-0)
    12. EPA Substance Registry System: trans-3-Methylcyclobutanecarboxylic acid(87863-09-0)
  • 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: 87863-09-0(Hazardous Substances Data)

87863-09-0 Usage

Uses

Used in Pharmaceutical Industry:
Trans-3-Methylcyclobutanecarboxylic acid is used as an intermediate in the synthesis of pharmaceuticals for its potential biological activities, making it a promising candidate for pharmaceutical research and development.
Used in Agrochemical Industry:
This chemical is also used as an intermediate in the synthesis of agrochemicals, contributing to the development of various agrochemical products.
Used in Polymer and Resin Production:
Trans-3-Methylcyclobutanecarboxylic acid serves as a building block in the production of various polymers and resins, playing a crucial role in the manufacturing process of these materials.
However, it is important to handle trans-3-Methylcyclobutanecarboxylic acid with care due to its corrosive nature and potential hazards to health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 87863-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,6 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87863-09:
(7*8)+(6*7)+(5*8)+(4*6)+(3*3)+(2*0)+(1*9)=180
180 % 10 = 0
So 87863-09-0 is a valid CAS Registry Number.

87863-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-3-Methylcyclobutancarbonsaeure

1.2 Other means of identification

Product number -
Other names trans-3-Methylcyclobutanecarboxylic 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:87863-09-0 SDS

87863-09-0Downstream Products

87863-09-0Relevant articles and documents

Synthesis of Stereoisomeric 3-Substituted Cyclobutanecarboxylic Acid Derivatives

Dehmlow, Eckehard V.,Schmidt, Stefan

, p. 411 - 414 (2007/10/02)

The preparation of 3-substituted cyclobutanecarboxylic acids by ring forming malonic ester cycloalkylation/saponification/decarboxylation leads to 50:50 cis/trans mixtures.Only some polar ester derivatives 2 can be separated by chromatographic methods.Catalytic hydrogenation of 3-substituted cyclobutanecarboxylic acids 3, however, gives the cis acids 4 with 90-95 percent selectivity.Reduction of the same acids 3 by Zn in aqueous HCl/THF leads to the trans acids 6 with 90-93 percent selectivity.

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