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2-Oxabicyclo[4.1.0]heptane, 7,7-dichloro- is a chemical compound with the molecular formula C7H8Cl2O. It is a derivative of bicycloheptane, a cyclic hydrocarbon, with an oxygen atom (oxa) incorporated into the structure and two chlorine atoms attached to the carbon atoms at the 7th position. 2-Oxabicyclo[4.1.0]heptane, 7,7-dichloro- is characterized by its unique bicyclic structure and the presence of both oxygen and chlorine atoms, which can influence its reactivity and properties. It is an example of a halogenated organic compound, which can have various applications in the chemical industry, such as in the synthesis of pharmaceuticals or as an intermediate in organic synthesis. The specific uses and properties of 2-Oxabicyclo[4.1.0]heptane, 7,7-dichloro- would depend on its stability, solubility, and reactivity, which are determined by its molecular structure.

7556-13-0

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7556-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7556-13-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,5 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7556-13:
(6*7)+(5*5)+(4*5)+(3*6)+(2*1)+(1*3)=110
110 % 10 = 0
So 7556-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H8Cl2O/c7-6(8)4-2-1-3-9-5(4)6/h4-5H,1-3H2

7556-13-0SDS

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 7,7-dichloro-5-oxabicyclo[4.1.0]heptane

1.2 Other means of identification

Product number -
Other names 2-Oxa-7,7-dichlor-norcaran

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:7556-13-0 SDS

7556-13-0Downstream Products

7556-13-0Relevant academic research and scientific papers

A facile procedure for the generation of dichlorocarbene from the reaction of carbon tetrachloride and magnesium using ultrasonic irradiation

Lin, Haixia,Yang, Mingfa,Huang, Peigang,Cao, Weiguo

, p. 608 - 613 (2007/10/03)

An improved method for the generation of dichlorocarbene was developed that utilizes ultrasound in the reaction of carbon tetrachloride with magnesium. High yields of gem-dichlorocyclopropane derivatives can be obtained in the presence of olefins by this method.

Synthesis and utility of α,α'-bis (triethyl ammonium methylene chloride) β-phenyl ethene in hydroxide ion initiated reactions - A new multi-site phase transfer catalyst

Balakrishnan,Jayachandran

, p. 3821 - 3830 (2007/10/03)

A three step synthesis of novel 'multi-site' water soluble phase transfer catalyst viz, α,α'-bis(triethyl ammonium methylene chloride) β-phenyl ethene and its utility in various organic biphase reactions are described.

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