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87863-09-0

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87863-09-0 Usage

General Description

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. This chemical is often used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a building block in the production of various polymers and resins. Additionally, trans-3-Methylcyclobutanecarboxylic acid exhibits potential biological activities, making it a potential candidate for pharmaceutical research and development. However, it is important to handle this chemical 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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