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CAS

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14845-41-1

6-Methylnorcaran-2-one is a colorless liquid chemical compound belonging to the family of norcarane derivatives, characterized by its faint floral odor.
Used in Fragrance Industry:
6-Methylnorcaran-2-one is used as a perfume and flavoring agent for its pleasant scent.
Used in Personal Care Products:
6-Methylnorcaran-2-one is used as a scent enhancer in the production of soaps, detergents, and other personal care products to provide a desirable fragrance.
Used in Pharmaceutical Industry:
6-Methylnorcaran-2-one has potential applications as a component in the development of new drugs and medications, although it requires careful handling due to its irritant properties.
Safety Note:
Prolonged exposure to 6-Methylnorcaran-2-one can lead to irritation of the eyes, skin, and respiratory system, so it is important to handle this chemical with care.

14845-41-1

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14845-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14845-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,4 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14845-41:
(7*1)+(6*4)+(5*8)+(4*4)+(3*5)+(2*4)+(1*1)=111
111 % 10 = 1
So 14845-41-1 is a valid CAS Registry Number.

14845-41-1SDS

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 6-methylbicyclo[4.1.0]heptan-2-one

1.2 Other means of identification

Product number -
Other names 6-Methylbicyclo<4.1.0>heptan-2-on

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:14845-41-1 SDS

14845-41-1Relevant articles and documents

POLYCYCLIC-CARBAMOYLPYRIDONE COMPOUNDS AND THEIR USE FOR THE TREATMENT OF HIV INFECTIONS

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Page/Page column 68; 69; 70, (2015/02/02)

Compounds for use in the treatment of human immunodeficiency virus (HIV) infection are disclosed. The compounds have the following Formula (I): (I) including stereoisomers and pharmaceutically acceptable salts thereof, wherein L, R1, R5/s

Photoinduced Electron Transfer Reactions of α-Cyclopropyl- And α-Epoxy Ketones. Tandem Fragmentation-Cyclization to Bi-, Tri-, and Spirocyclic Ketones

Kirschberg, Thorsten,Mattay, Jochen

, p. 8885 - 8896 (2007/10/03)

Reductive photoinduced electron transfer (PET) reactions have been performed with various bicyclic a-cyclopropyl-substituted ketones and tertiary amines. The reaction resulted in a regioselective cleavage of one cyclopropyl bond under formation of an exocyclic radical with an endocyclic enolate unit. In the case of bicyclic ketones with an unsaturated side chain, various bicyclic, spirocyclic, and tricyclic products are accessible via radical cyclization, depending on the position of the alkenyl substituent. In addition to triethylamine, W-silylated amines have also been used as electron donors, leading to a variety of compounds, among them are silylated fragmentation products, indicating that a proton is transferred from not only the amine radical cation but also the cationic silyl group. The intramolecular Paternoe-Buechi reaction has also been studied for cyclopropane derivatives of the jasmone type leading to tetracyclic oxetanes. Finally, α-epoxy-substituted ketones have been investigated under PET conditions, yielding ring-opened products.

Chemical Transformation of Terpenoids. VII. Syntheses of Chiral Segments, Key Building-Blocks for the Right Half of Taxane-Type Diterpenoids

Shibuya, Hirotaka,Tsujii, Shinji,Yamamoto, Yoshio,Miura, Hiromi,Kitagawa, Isao

, p. 3417 - 3427 (2007/10/02)

Two kinds of chiral segments, i.e. segment B-I (4) and segment B-II (5), which are potentially versatile building-blocks for construction of the right half of taxane-type diterpenoids, were synthesized from 3-methyl-2-cyclohexen-1-one (6) via optical reso

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