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7,7-Dimethoxybicyclo(2,2,1)heptene is a chemical compound with the molecular formula C9H14O2. It is a colorless liquid with a fruity, floral odor. 7,7-Dimethoxybicyclo(2,2,1)heptene is a member of the bicycloheptene family and is characterized by the presence of two oxygen atoms bonded to the carbon atoms at positions 7 and 7, which are part of a seven-membered ring structure. It is used as a fragrance ingredient in various personal care products, such as perfumes and cosmetics, due to its pleasant scent. The compound is also known for its potential applications in the synthesis of other organic compounds, particularly in the pharmaceutical and chemical industries.

875-04-7

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875-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 875-04-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 875-04:
(5*8)+(4*7)+(3*5)+(2*0)+(1*4)=87
87 % 10 = 7
So 875-04-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O2/c1-10-9(11-2)7-3-4-8(9)6-5-7/h3-4,7-8H,5-6H2,1-2H3

875-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,7-dimethoxybicyclo[2.2.1]hept-2-ene

1.2 Other means of identification

Product number -
Other names 7,7-dimethoxynorbornene

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:875-04-7 SDS

875-04-7Relevant academic research and scientific papers

An Unusual Occurrence of Chemiluminescence resulting from Metal-Ammonia Reductive Dehalogenation Reactions

Cotsaris, Evangelo,Paddon-Row, Michael N.

, p. 95 - 96 (2007/10/02)

Birch type reductive dehalogenation of some members of the series of norbornenes (2a - h), (4i) proceeds with chemiluminescence; an explanation for this phenomenon is advanced.

The Octant Rule. 7. Deuterium as an Octant Pertuber

Lightner, David A.,Gawronski, Jacek K.,Bouman, Thomas D.

, p. 1983 - 1990 (2007/10/02)

(1S)-exo-2-Deuteriobicycloheptan-7-one (1) and (1S)-endo-2-deuteriobicycloheptan-7-one (2) were synthesized, and their circular dichroism spectra were measured and analyzed.Both ketones show dissignate Cotton effects near 295 nm corresponding to their n-?* electronic transitions: 1 (Δε296 = +0.033) and 2 (Δε292 = +0.132).The nature of the isotopic perturbation on the n-?* transitions of 1 and 2, related β-deuterioadamantanones and cyclohexanones, and α-deuteriocyclohexanones is treated theoretically.The net contribution to the sign of the rotatory strength is determined by the relatively more consignate contribution on the C-H bond that is located in an oppositely signed octant relative to the C-D bond.

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