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1,2,3-Cyclopropanetri-carboxylic acid is a tricarboxylic acid featuring a cyclopropane ring structure. It is a colorless crystalline compound with the molecular formula C6H6O6. This chemical compound is utilized in various applications, including organic synthesis, pharmaceutical and agrochemical production, polymer manufacturing, and specialty chemical development.

705-35-1

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705-35-1 Usage

Uses

Used in Organic Synthesis:
1,2,3-Cyclopropanetri-carboxylic acid serves as a key intermediate in organic synthesis, facilitating the creation of a wide range of compounds with diverse applications across various industrial and scientific fields.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1,2,3-cyclopropanetri-carboxylic acid is used as a building block for the development of various drugs. Its unique structure and reactivity contribute to the synthesis of medicinal compounds with potential therapeutic benefits.
Used in Agrochemical Production:
Similarly, in agrochemical manufacturing, 1,2,3-cyclopropanetri-carboxylic acid is employed as a fundamental component in the synthesis of crop protection agents and other agricultural products, enhancing crop yield and protection.
Used in Polymer Manufacturing:
1,2,3-Cyclopropanetri-carboxylic acid is also utilized in the production of polymers, contributing to the development of materials with specific properties for use in various applications.
Used in Specialty Chemicals:
1,2,3-cyclopropanetri-carboxylic acid is further employed in the creation of specialty chemicals, which are tailored for particular industries and applications, showcasing the versatility of 1,2,3-cyclopropanetri-carboxylic acid in chemical development.
Used in Materials Science:
1,2,3-Cyclopropanetri-carboxylic acid has applications in the field of materials science, where it is researched for its potential use in drug delivery systems and biomaterials, highlighting its importance in advancing modern scientific and medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 705-35-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 705-35:
(5*7)+(4*0)+(3*5)+(2*3)+(1*5)=61
61 % 10 = 1
So 705-35-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O6/c7-4(8)1-2(5(9)10)3(1)6(11)12/h1-3H,(H,7,8)(H,9,10)(H,11,12)

705-35-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-Cyclopropane-1,2,3-tricarboxylic acid

1.2 Other means of identification

Product number -
Other names cis,trans-1.2.3-Cyclopropantricarbonsaeure

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:705-35-1 SDS

705-35-1Relevant academic research and scientific papers

Enantiodivergent syntheses of (-)- and (+)-dysibetaine CPa and N-desmethyl analog

Sakai, Michihiro,Tanaka, Kento,Takamizawa, Satoshi,Oikawa, Masato

, p. 4587 - 4594 (2014/06/23)

The first total syntheses of (-)-dysibetaine CPa and the antipode have been achieved using enantioselective solvolysis of meso-cyclic anhydride mediated by quinine derivative as an organocatalyst. The synthesis features a demonstration of an enantiodiverg

First enantioselective total synthesis of (-)-dysibetaine CPa and absolute configurations of natural product

Sakai, Michihiro,Ishikawa, Yuichi,Takamizawa, Satoshi,Oikawa, Masato

, p. 5911 - 5912 (2013/10/21)

Here we report total synthesis of enantiomerically pure dysibetaine CPa, isolated from Micronesian marine sponge and expected to serve as a neuroactive agent. Starting from meso-cyclopropane triester, the synthesis was achieved in 12.8% overall yield over

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