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5-Hexen-2-one, 3-methylene- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52358-87-9

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52358-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52358-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,5 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52358-87:
(7*5)+(6*2)+(5*3)+(4*5)+(3*8)+(2*8)+(1*7)=129
129 % 10 = 9
So 52358-87-9 is a valid CAS Registry Number.

52358-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylene-5-hexen-2-one

1.2 Other means of identification

Product number -
Other names 3-methylenehex-5-en-2-one

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:52358-87-9 SDS

52358-87-9Relevant academic research and scientific papers

The bidirectional total synthesis of sampsonione P and hyperibone i

Lindermayr, Katharina,Plietker, Bernd

supporting information, p. 12183 - 12186 (2013/12/04)

Make it simple: The separation of framework-decorating from framework-constructing steps facilitated the selective introduction of one prenyl group next to allyl groups. The selective epoxidation of the more electron-rich prenyl group led to the efficient formation of the tetrahydrofuran moiety in the title compounds. Spectroscopic analysis of hyperiboneI and comparison with literature data led to a revision of the original structure. Copyright

Synthesis and biological evaluation of 3-alkyl-dihydrotetrabenazine derivatives as vesicular monoamine transporter-2 (VMAT2) ligands

Zheng, Pinguan,Lieberman, Brian P.,Choi, Seok Rye,Pl?essl, Karl,Kung, Hank F.

supporting information; experimental part, p. 3435 - 3438 (2011/06/24)

In the search of new probes for in vivo brain imaging of vesicular monoamine transporter type 2 (VMAT2), we have developed an efficient synthesis of a novel series of 3-alkyl-dihydrotetrabenazine (DTBZ) derivatives. The affinity of VMAT2 was evaluated by an in vitro inhibitory binding assay using [125I]-iodovinyl-TBZ or [18F](+)-FP-DTBZ as radioligands in rat striatal tissue homogenates. New DTBZ derivatives exhibited moderate to good binding affinity to VMAT2. Among these new ligands, compound 4b showed the best affinity for VMAT2 (Ki = 5.98 nM) and may be a useful lead compound for future structure-activity studies.

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