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16294-60-3

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16294-60-3 Usage

General Description

(3-Acenaphthoyl)propionic acid is a chemical compound that consists of a propionic acid group attached to the 3-position of an acenaphthoyl moiety. It is used in organic synthesis and research as a building block for the preparation of biologically active molecules and pharmaceuticals. The compound is known for its role in the modification of natural products, leading to the development of novel drugs and therapeutic agents. Additionally, (3-Acenaphthoyl)propionic acid has potential applications in the fields of materials science and chemical technology due to its unique structural features and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 16294-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,9 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16294-60:
(7*1)+(6*6)+(5*2)+(4*9)+(3*4)+(2*6)+(1*0)=113
113 % 10 = 3
So 16294-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H14O3/c17-14(8-9-15(18)19)12-7-6-11-5-4-10-2-1-3-13(12)16(10)11/h1-3,6-7H,4-5,8-9H2,(H,18,19)

16294-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,2-dihydroacenaphthylen-5-yl)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names 4-Acenaphthen-5-yl-4-oxo-buttersaeure

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:16294-60-3 SDS

16294-60-3Relevant articles and documents

-

Fieser

, p. 1 (1940)

-

Condensed Heterocycles : Part VI - Synthesis of Dihydroacephenanthro-thiazoles, -isoxazole and -pyrazoles and Dihydroacenaphthocarbazoles

Kumar, Satish,Singh, Vijander,Sharma, K. S.

, p. 542 - 545 (2007/10/02)

1-Oxo-1,2,3,4-tetrahydroacephenanthrene (I) has been converted to 2-amino-10,11-dihydroacephenanthrothiazole (III), 14(H)-aza-12,13-dihydroacenaphthocarbazole (IV), 10,11-dihydro-2-hydrazinoacephenanthrothiazole (V), 10,11-dihydroacephenanthroisoxazole (VII), 10,11-dihydroacephenanthropyrazole (VIII), 10,11-dihydro-3-phenylacephenanthropyrazole (IX), 10,11-dihydro-3-thiocarbamoylacephenanthropyrazole (X) and 12,13-dihydroacenaphthocarbazole (XII).

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