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tricyclo[4.2.0.0~2,5~]oct-3-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39781-76-5

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39781-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39781-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,8 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39781-76:
(7*3)+(6*9)+(5*7)+(4*8)+(3*1)+(2*7)+(1*6)=165
165 % 10 = 5
So 39781-76-5 is a valid CAS Registry Number.

39781-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name AC1L3KZX

1.2 Other means of identification

Product number -
Other names Dihydro-anti-tricyclo<4.1.0.02,5>octa-3,7-dien

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:39781-76-5 SDS

39781-76-5Downstream Products

39781-76-5Relevant academic research and scientific papers

Enantioselective synthesis of pentacycloanammoxic acid

Mascitti, Vincent,Corey

, p. 3118 - 3119 (2007/10/03)

A highly effective enantioselective synthesis of pentacycloanammoxic acid (1), an unusual naturally occurring fatty acid from Candidatus Brocadia anammoxidans, has been accomplished. The C20-structure of 1 was assembled with stereocontrol from four building blocks, cyclobutene, 2-cyclopentenone, the chiral silylcyclopentenone 6, and 7-bromoheptanoic acid. Both 1 and its enantiomer are now available in quantities that should facilitate future studies on the mode of biosynthesis which appears to be unprecedented. Copyright

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