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1,4,5,6-tetrachloro-7,7-dimethoxybicyclo[2.2.1]hept-5-en-2-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40001-91-0

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40001-91-0 Usage

Structure

Bicyclic compound with four chlorine atoms, two methoxy groups, and an acetate group attached to the carbon ring

Functional Groups

Chlorine atoms, methoxy groups, and an acetate group

Potential Applications

Industrial and research applications

Synthesis

Likely synthesized through organic synthesis methods, using the bicyclic compound as a starting material and introducing the chlorine, methoxy, and acetate groups

Physical Properties

Unknown, but may include appearance, density, melting point, and boiling point

Chemical Properties

Unknown, but may include reactivity, stability, and solubility

Hazards

Unknown, but may include toxicity, flammability, and environmental impact

Further Research

Additional research and testing needed to determine specific properties, applications, and potential hazards

Check Digit Verification of cas no

The CAS Registry Mumber 40001-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,0,0 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40001-91:
(7*4)+(6*0)+(5*0)+(4*0)+(3*1)+(2*9)+(1*1)=50
50 % 10 = 0
So 40001-91-0 is a valid CAS Registry Number.

40001-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1,2,3,4-tetrachloro-7,7-dimethoxy-5-bicyclo[2.2.1]hept-2-enyl) acetate

1.2 Other means of identification

Product number -
Other names (+/-)-(1R,2S,4S)-1,4,5,6-tetrachloro-7,7-dimethoxybicyclo[2.2.1]hept-5-en-2-yl acetate

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:40001-91-0 SDS

40001-91-0Relevant academic research and scientific papers

Robust synthesis of enantiopure cyclohexenyl analogues of 2/3-deoxyribose sugars as carbocyclic nucleoside precursors

Varada, Manojkumar,Kotikam, Venubabu,Kumar, Vaijayanti A.

experimental part, p. 5744 - 5749 (2011/08/21)

An expedient synthesis of 2-deoxy (10) and 3-deoxy (11) cyclohexenyl analogues of 2-deoxy and 3-deoxy-d-ribose sugar from commercially available starting materials is reported. Highly efficient enzymatic resolution of the key compound 10 is described usin

Microwave-assisted solvent-free Diels-Alder reaction - A fast and simple route to various 5,6-substituted norbornenes and polychlorinated norbornenes

Dejmek, Milan,Hrebabecky, Hubert,Sala, Michal,Drainsky, Martin,Nencka, Radim

experimental part, p. 4077 - 4083 (2012/01/05)

A series of 5,6-substituted norbornenes and 5,6-substituted polychlorinated norbornenes was prepared by using a microwave-assisted Diels-Alder reaction. This procedure proved very versatile, fast, and with an easy workup step, and therefore suitable even for large-scale synthesis. Georg Thieme Verlag Stuttgart · New York.

Synthetic studies related to CP-225,917

Clive, Derrick L.J.,Sgarbi, Paulo W.M.,He, Xiao,Sun, Shaoyi,Zhang, Junhu,Ou, Ligong

, p. 811 - 824 (2007/10/03)

Synthetic studies related to CP-225,917 are described, including the preparation of the fully oxygenated tetracyclic central core 3.

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