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6-BUTYL[1,2,3,4-TETRAHYDRONAPHTHALENE] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30654-45-6

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30654-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30654-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,5 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30654-45:
(7*3)+(6*0)+(5*6)+(4*5)+(3*4)+(2*4)+(1*5)=96
96 % 10 = 6
So 30654-45-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H20/c1-2-3-6-12-9-10-13-7-4-5-8-14(13)11-12/h9-11H,2-8H2,1H3

30654-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-n-Butyl-[1,2,3,4-tetrahydronaphthalene]

1.2 Other means of identification

Product number -
Other names 6-Butyl-1,2,3,4-tetrahydro-naphthalin

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:30654-45-6 SDS

30654-45-6Upstream product

30654-45-6Downstream Products

30654-45-6Relevant academic research and scientific papers

Reduction of Polycyclic Arenes by BH Boranes, III. Partial Hydrogenation: From Anthracene to Coronene

Yalpani, Mohamed,Koester, Roland

, p. 719 - 724 (2007/10/02)

Tetrapropyldiboran(6) (TPDB) katalysiert die Hydrierung polycyclischer Arene unter Wasserstoff-Druck bei bei 200 deg C.In einigen Faellen koennen sehr hohe Ausbeuten an Hydroarenen erzielt werden .Neben unterschiedlichen kleinen Mengen an Perhydroarenen bilden sich nach langer Reaktionszeit aus saemtlichen Arenen auch C-C-Spaltungsprodukte.

Synthesis and Dediazoniation of 2-Butyl- and 2,5-Dibutylbenzenediazonium Ions

Sikkar, Rein,Martinson, Per

, p. 551 - 558 (2007/10/02)

2-Butylbenzenediazonium ion (1a) and 2,5-dibutylbenzenediazonium ion (1b) have been thermally decomposed in aqueous acid solution.In addition to the major product, the corresponding phenol, 5- and 6-membered ring products are formed (in a ratio of ca. 7:1) as well as products of elimination and substitution in the o-butyl group.The formation of the non-phenolic products is explained in terms of competing reactions of the initially formed aryl cations: cyclization by electrophilic atttack on the o-butyl group and 1,5-hydride ion transfer from the o-butyl group with concomitant elimination or reaction with the medium.Decompositions of 1a in the presence of copper(I) oxide, believed to generate aryl radicals, does not yield any measurable quantities of cyclized products, however.

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