62614-70-4

Basic information

• Product Name: CIS-6-CHLORO-2-HEXENE
• Synonyms: CIS-4-HEXEN-1-YL CHLORIDE;CIS-6-CHLORO-2-HEXENE;Chlorohexene;cis-6-chloro-2-hexene90+%
• CAS NO: 62614-70-4
• Molecular Formula: C₆H₁₁Cl
• Molecular Weight: 118.6
• Mol File: 62614-70-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 132 °C
• Appearance: /
• Density: 0.92
• Refractive Index: 1.4420-1.4450
• CAS DataBase Reference: CIS-6-CHLORO-2-HEXENE(CAS DataBase Reference)
• NIST Chemistry Reference: CIS-6-CHLORO-2-HEXENE(62614-70-4)
• EPA Substance Registry System: CIS-6-CHLORO-2-HEXENE(62614-70-4)

Safety Data

• RIDADR: 1993
• Hazardous Substances Data: 62614-70-4(Hazardous Substances Data)

Usage

General Description

CIS-6-CHLORO-2-HEXENE, also known as cis-6-chlorohex-2-ene, is a chemical compound with the molecular formula C6H11Cl. It is a colorless liquid with a strong, pungent odor, and is classified as an alkene due to its double carbon-carbon bond. CIS-6-CHLORO-2-HEXENE is primarily used as an intermediate in the synthesis of various organic compounds, such as pharmaceuticals, agrochemicals, and other specialty chemicals. It is also used in the production of polymers and as a solvent for various industrial applications. However, CIS-6-CHLORO-2-HEXENE is considered to be toxic if inhaled, causing irritation to the respiratory system, and is harmful if swallowed or comes into contact with the skin, causing irritation and burns. Therefore, it is important to handle this chemical with care and follow proper safety precautions when working with it.

InChI:InChI=1/C6H11Cl/c1-2-3-4-5-6-7/h2-3H,4-6H2,1H3/b3-2-

Upstream product

• 629-11-8 1,6-hexanediol 
• 6126-50-7 hex-4-en-1-ol 
• 928-89-2 6-chlorohexene 
• 928-92-7 (E)-hex-4-en-1-ol 
• 28077-73-8 6-chlorohex-2-yne 
• 928-91-6 (Z)-4-hexenol 
• 821-41-0 5-Hexen-1-ol 
• 928-93-8 4-hexyn-1-ol 
• 14267-92-6 1-chloro-4-pentyne 

Downstream Products

• 70681-89-9 ((E)-3-Hex-4-enyl)-cyclohex-2-enol 
• 2931-10-4 2-ethylcyclopent-2-en-1-one 
• 1121-18-2 2-methyl-2-cyclohexen-1-one 
• 105-21-5 4-propylbutanolide 
• 70681-91-3 3-<(E)-4-hexenyl>-2-cyclohexen-1-one 

Relevant articles and documents

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Benign catalysis with iron: Unique selectivity in catalytic isomerization reactions of olefins

The use of noble metal catalysts in homogeneous catalysis has been well established. Due to their price and limited availability, there is growing interest in the substitution of such precious metal complexes with readily available and bio-relevant catalysts. In particular, iron is a "rising star" in catalysis. Herein, we present a general and selective iron-catalyzed monoisomerization of olefins, which allows for the selective generation of 2-olefins. Typically, common metal complexes give mixtures of various internal olefins. Both bulk-scale terminal olefins and functionalized terminal olefins give the corresponding products under mild conditions in good to excellent yields. The proposed reaction mechanism was elucidated by in situ NMR studies and supported by DFT calculations and extended X-ray absorption fine structure (EXAFS) measurements.

Medicaments, vicinal dihydroxyalkylxanthines contained therein, processes for the preparation of these xanthine compounds and intermediate products suitable for these

Compounds of the formula STR1 wherein one of the radicals R1, R2 or R3 denotes a straight-chain alkyl group having 4 to 8 C atoms and two vicinal hydroxyl groups in the ω,ω-1 or ω-1,ω-2 positions and the two other radicals represent straight-chain or branched alkyl groups having up to 12 C atoms in the position of R1 and R3 and up to 4 C atoms in the position of R2, the total of C atoms in these two alkyl substituents being a maximum of 14, are prepared by oxidation of the corresponding alkenylxanthines and by alkylation with compounds which introduce the dihydroxyalkyl radical or a precursor thereof. The dihydroxyalkyldialkylxanthines are suitable for the treatment of obstructive respiratory tract diseases.