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"2H-Oxocin-3(6H)-one,7,8-dihydro-(8CI,9CI)" is a complex chemical compound with the molecular formula C7H6O3. It belongs to the class of organic compounds known as oxocins, which are characterized by a cyclohexanone ring with a carbonyl group at position 3. This specific compound features a 7,8-dihydro structure, indicating that the carbon atoms at positions 7 and 8 are connected by a single bond, resulting in a saturated ring system. The compound is also referred to by its IUPAC name, which provides a standardized way to name organic compounds based on their structure. It is important to note that the compound's properties, such as reactivity and solubility, are influenced by its molecular structure and the presence of functional groups.

29425-60-3

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29425-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29425-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,2 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29425-60:
(7*2)+(6*9)+(5*4)+(4*2)+(3*5)+(2*6)+(1*0)=123
123 % 10 = 3
So 29425-60-3 is a valid CAS Registry Number.

29425-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,8-dihydro-6H-oxocin-3-one

1.2 Other means of identification

Product number -
Other names 7,8-Dihydro-2H-oxarin-3(6H)-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:29425-60-3 SDS

29425-60-3Downstream Products

29425-60-3Relevant academic research and scientific papers

Synthesis of 3-oxooxa- and 3-oxoazacycloalk-4-enes by ring-closing metathesis. Application to the synthesis of an inhibitor of cathepsin K

Taillier, Catherine,Hameury, Thomas,Bellosta, Véronique,Cossy, Janine

, p. 4472 - 4490 (2008/02/01)

3-Oxooxa- and 3-oxoazacycloalk-4-enes were obtained with good yield from 1-(ω-alkenyloxy)- and 1-(ω-alkenylamino)-but-3-en-2-ones by using a ring-closing metathesis. This methodology has been used to synthesize an inhibitor of cathepsin K.

Synthesis of 3-oxo oxacycloalkenes by ring closing metathesis

Cossy, Janine,Taillier, Catherine,Bellosta, Véronique

, p. 7263 - 7266 (2007/10/03)

The synthesis of six-, seven- and eight-membered 3-oxo oxacycloalkenes by using ring-closing metathesis has been achieved from 1-(ω-alkenyloxy)-but-3-en-2-ones.

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