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635-08-5

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635-08-5 Usage

Description

3,4,5,6-tetrahydrophthalic acid, also known as cis-4-cyclohexene-1,2-dicarboxylic acid, is a cyclohexene carboxylic acid with the molecular formula C8H10O4. It is a white crystalline solid that is widely used in the production of various polymers, resins, and other industrial products. It also serves as a building block in organic synthesis for the preparation of more complex chemical compounds and is utilized in the pharmaceutical industry for the synthesis of certain drugs. However, it is important to handle this compound with caution due to its potential hazards if not handled properly.

Uses

Used in Polymer and Resin Production:
3,4,5,6-tetrahydrophthalic acid is used as a monomer for the production of various polymers and resins. Its unique structure and properties make it suitable for creating materials with specific characteristics, such as improved strength, flexibility, and chemical resistance.
Used in Organic Synthesis:
3,4,5,6-tetrahydrophthalic acid is used as a building block in organic synthesis for the preparation of more complex chemical compounds. Its versatile structure allows for the synthesis of a wide range of compounds, making it a valuable intermediate in the chemical industry.
Used in Pharmaceutical Industry:
3,4,5,6-tetrahydrophthalic acid is used as a starting material in the synthesis of certain drugs. Its unique properties and reactivity make it a valuable component in the development of new pharmaceuticals.
Used in Chemical Intermediates:
3,4,5,6-tetrahydrophthalic acid is used as a chemical intermediate in the production of various industrial products. Its versatility and reactivity make it a key component in the synthesis of a wide range of compounds, contributing to the development of new technologies and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 635-08-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 635-08:
(5*6)+(4*3)+(3*5)+(2*0)+(1*8)=65
65 % 10 = 5
So 635-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H2,(H,9,10)(H,11,12)

635-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohex-1-ene-1,2-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names Cyclohex-1-en-1,2-dicarbonsaeure

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:635-08-5 SDS

635-08-5Relevant articles and documents

Variable-temperature study of hydrogen-bond symmetry in cyclohexene-1,2-dicarboxylate monoanion in chloroform-d

Perrin, Charles L.,Burke, Kathryn D.

supporting information, p. 4355 - 4362 (2014/04/03)

The symmetry of the hydrogen bond in hydrogen cyclohexene-1,2-dicarboxylate monoanion was determined in chloroform using the NMR method of isotopic perturbation. As the temperature decreases, the 18O-induced 13C chemical-shift separations increase not only at carboxyl carbons but also at ipso (alkene) carbons. The magnitude of the ipso increase is consistent with an 18O isotope effect on carboxylic acid acidity. Therefore it is concluded that this monoanion is a mixture of tautomers in rapid equilibrium, rather than a single symmetric structure in which a chemical-shift separation arises from coupling between a desymmetrizing vibration and anharmonic isotope-dependent vibrations, which is expected to show the opposite temperature dependence.

On the mechanism of oxidation of trans-decahydronaphthalene at 100

McARTHUR,SMITH

, p. 43 - 60 (2007/12/05)

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