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tricyclo[3.3.1.0~2,8~]nona-3,6-diene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14693-11-9

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14693-11-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14693-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,9 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14693-11:
(7*1)+(6*4)+(5*6)+(4*9)+(3*3)+(2*1)+(1*1)=109
109 % 10 = 9
So 14693-11-9 is a valid CAS Registry Number.

14693-11-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Tricyclo[3.3.1.02,8]nona-3,6-diene

1.2 Other means of identification

Product number -
Other names Tricyclo<3.3.1.02,8>nona-3,6-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:14693-11-9 SDS

14693-11-9Downstream Products

14693-11-9Relevant academic research and scientific papers

Tricyclo2,8>nona-3,6-dienyl and bicyclonona-2,6,8-trienyl; A Fluxional Radical Pair

Walton, John C.

, p. 468 - 469 (1989)

Tricyclo2,8>nona-3,6-dienyl and bicyclonona-2,6,8-trienyl radicals form a pair which is rendered fluxional by a series of degenerate cyclopropylmethyl type rearrangements.

PHOTOREACTIONS OF 2,3-DIAZATETRACYCLOUNDECA-2,9-DIENES; THE RETRO-1,3-DIPOLAR CYCLOADDITIONS AND THE NITROGEN EXTRUSION REACTIONS

Kumagai, Tsutomu,Ohba, Yoshihiro,Mukai, Toshio

, p. 439 - 442 (2007/10/02)

The photochemical reactions of tetracyclic azo compounds (1a-b) giving 5a-b and 8a-b via diazoethane derivatives (6a-b) were investigated in addition to the nitrogen extrusion reactions leading to tetracyclononenes (4a-b).

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