55682-98-9

Basic information

• Product Name: 3-Chloro-1-heptene
• Synonyms: 3-Chloro-1-heptene
• CAS NO: 55682-98-9
• Molecular Formula: C₇H₁₃Cl
• Molecular Weight: 132.63
• Mol File: 55682-98-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 163.46°C (estimate)
• Appearance: /
• Density: 0.9212 (estimate)
• Refractive Index: 1.4282 (estimate)
• CAS DataBase Reference: 3-Chloro-1-heptene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Chloro-1-heptene(55682-98-9)
• EPA Substance Registry System: 3-Chloro-1-heptene(55682-98-9)

Safety Data

• Hazardous Substances Data: 55682-98-9(Hazardous Substances Data)

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 46, p. 1504, 1981 DOI: 10.1021/jo00320a058

Upstream product

• 109-65-9 1-bromo-butane 
• 113662-35-4 (Z-3-chloroprop-2-enyl)tri-n-butyl stannane 
• 110-86-1 pyridine 
• 4938-52-7 (3R)-1-hepten-3-ol 
• 7719-12-2 phosphorus trichloride 
• 4938-52-7 1-hepten-3-ol 
• 60-29-7 diethyl ether 
• 10026-13-8 phosphorus pentachloride 
• 100594-85-2 (-)(R)-3-bromo-heptene-⁽¹⁾ 
• 67-56-1 methanol 
• 4938-52-7 (S)-Hept-1-en-3-ol 
• 592-76-7 1-Heptene 
• 563-52-0 2-chloro-3-butene 
• 22104-77-4 hept-2-en-1-ol 

Downstream Products

• 32653-33-1 (S)-α-Chlor-n-capronsaeure 
• 999-52-0 (+)(S)-3-chloro-heptane 
• 1322084-84-3 C₁₇H₂₃ClO 

Relevant articles and documents

Addition of CCl4 to olefins catalyzed by chromium and ruthenium complexes: The influence of water as a nucleophilic additive

The feasibility of the addition of CCl4 to linear and cyclic olefins and dienes in the presence of chromium and ruthenium complexes was established. The influence of water as a nucleophilic additive and the influence of the olefin nature, the c

PROCESS FOR PRODUCING 2-OXO-3-AROMATIC CARBOXYLIC ACID DERIVATIVES

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ETUDE DE L'ALKYLATION D'ORGANOLITHIENS ALLYLIQUES MONOCHLORES: SYNTHESE EN UNE ETAPE DE CHLORURES ALLYLIQUES SECONDAIRES OU TERTIAIRES ET/OU DE CHLORURES VINYLIQUES DE CONFIGURATION Z

Chloroallyllithium and gem-chloro(methyl)allyllithium readily react with various alkylating reagents to produce, in a "one-pot" reaction, secundary or tertiary allylic chlorides and/or vinylic chlorides of Z configuration.