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54717-80-5

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54717-80-5 Usage

General Description

(1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl 3-oxobutanoate is a chemical compound with a complex molecular structure. It is a derivative of bicyclo[2.2.1]heptane and contains a 3-oxobutanoate functional group. (1R,2R,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl 3-oxobutanoate is a bicyclic terpene derivative, and it is commonly used in the fragrance and flavor industry. It has a unique and pleasant aroma and is often used as a fragrance ingredient in perfumes, colognes, and other scented products. Additionally, it may also have potential applications in pharmaceuticals and agrochemicals due to its interesting chemical properties and structural characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 54717-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,1 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54717-80:
(7*5)+(6*4)+(5*7)+(4*1)+(3*7)+(2*8)+(1*0)=135
135 % 10 = 5
So 54717-80-5 is a valid CAS Registry Number.

54717-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) 3-oxobutanoate

1.2 Other means of identification

Product number -
Other names 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl 3-oxobutanoate

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:54717-80-5 SDS

54717-80-5Upstream product

54717-80-5Downstream Products

54717-80-5Relevant articles and documents

Synthesis and pharmacological activities of calcium modulatory hexahydroquinolinones

Rose

, p. 199 - 203 (2007/10/02)

Hexahydroquinolinones of type 6 are accessible from Hantzsch-like cyclization of 1,3-cyclohexanedione with aromatic aldehydes and different β-aminocrotonates and acetoacetates/ammonia, respectively. Reaction with pyridiniumbromideperbromide leads to the octahydrofuro[3,4-b] quinoline-diones 6h and 6i. 6j was obtained by N-alkylation. Positive inotropic effects were observed on electrically stimulated left atria of guinea pigs whereas BaCl2-induced contractions of the ileum were inhibited in a dose dependent manner. On electrically stimulated guinea pig papillary muscle 6h exhibits contractility promoting effects which can be attributed to calcium agonism.

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