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1,4-Dioxaspiro[4.5]decan-8-yl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76297-05-7

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76297-05-7 Usage

Type of compound

Benzoate ester

Usage

Fragrance ingredient in consumer products (perfumes, lotions, soaps)

Structure

Spiro carbon ring and a benzoate group

Property

Pleasant odor

Suitability

Cosmetic and personal care products

Safety

Use with caution and in accordance with safety guidelines

Health risks

Potential risks with excessive or prolonged exposure

Check Digit Verification of cas no

The CAS Registry Mumber 76297-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,9 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76297-05:
(7*7)+(6*6)+(5*2)+(4*9)+(3*7)+(2*0)+(1*5)=157
157 % 10 = 7
So 76297-05-7 is a valid CAS Registry Number.

76297-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-DIOXASPIRO[4.5]DECAN-8-YLBENZOATE

1.2 Other means of identification

Product number -
Other names -

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:76297-05-7 SDS

76297-05-7Relevant academic research and scientific papers

Facile synthesis of N-substituted amides from alkenes and amides by a Bronsted acid mediated electrophilic addition reaction

Mihara, Karin,Okada, Iku,Chiba, Kazuhiro,Kitano, Yoshikazu

, p. 1455 - 1462 (2014/06/10)

A facile and widely applicable method for the synthesis of N-substituted amides from alkenes and amides using Bronsted acids was developed. Treatment of various alkenes with amides and an alkali metal halide or methanesulfonic acid in trifluoroacetic acid afforded the corresponding N-substituted amides in good to high yield. The reaction proceeds via the direct electrophilic addition of the amides to the alkenes. Various functional groups such as ester, ether, imide, amide, and halogen were tolerated under the reaction conditions. High substrate-dependent cis stereoselectivity in the synthesis was also observed for methylenecyclohexane and methylcyclohexene derivatives possessing a substituent at the 4-position. Furthermore, a practical application of this reaction has been demonstrated by the synthesis of an intermediate of a bioactive compound on a large scale. Georg Thieme Verlag Stuttgart New York.

Novel Compounds for the Treatment of Diseases Associated with Amyloid or Amyloid-Like Proteins

-

, (2011/11/30)

The present invention relates to novel compounds that can be employed in the treatment of a group of disorders and abnormalities associated with amyloid protein, such as Alzheimer's disease, and of diseases or conditions associated with amyloid-like proteins. The compounds of the present invention can also be used in the treatment of ocular diseases associated with pathological abnormalities/changes in the tissues of the visual system. The present invention further relates to pharmaceutical compositions comprising these compounds and to the use of these compounds for the preparation of medicaments for treating or preventing diseases or conditions associated with amyloid and/or amyloid-like proteins. A method of treating or preventing diseases or conditions associated with amyloid and/or amyloid-like proteins is also disclosed.

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