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27351-96-8

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27351-96-8 Usage

Family

Naphthalene compounds

Physical State

Colorless liquid

Odor

Mild

Common Use

Solvent in various industrial processes

Stability

Excellent

Volatility

Low

Suitability

Applications requiring high thermal and chemical resistance

Utilization

Key ingredient in the production of specialty chemicals

Examples of Specialty Chemicals

Surfactants, lubricants, and detergents

Additional Use

Carrier solvent for chemical reactions and formulations

Industry

Chemical industry

Versatility

High

Value

Valuable component in the chemical industry

Check Digit Verification of cas no

The CAS Registry Mumber 27351-96-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,5 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27351-96:
(7*2)+(6*7)+(5*3)+(4*5)+(3*1)+(2*9)+(1*6)=118
118 % 10 = 8
So 27351-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H20/c1-11(2)13-7-5-10-16-14(12(3)4)8-6-9-15(13)16/h5-12H,1-4H3

27351-96-8SDS

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 1,5-di(propan-2-yl)naphthalene

1.2 Other means of identification

Product number -
Other names 1,5-Bis(isopropyl)naphthalene

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:27351-96-8 SDS

27351-96-8Downstream Products

27351-96-8Relevant articles and documents

The isopropylation of naphthalene over USY zeolite with FAU topology. The selectivities of the products

Sugi, Yoshihiro,Joseph, Stalin,Ramadass, Kavitha,Indirathankam, Sathish Clastinrusselraj,Premkumar, Selvarajan,Dasireddy, Venkata D.B.C.,Yang, Jae-Hun,Al-Muhtaseb, Alaa H.,Liu, Qing,Kubota, Yoshihiro,Komura, Kenichi,Vinu, Ajayan

, p. 606 - 615 (2021/03/31)

The isopropylation of naphthalene (NP) over USY zeolite (FAU06, SiO2/Al2O3 = 6) gave all eight possible diisopropylnaphthalene (DIPN) isomers: β,β- (2,6- and 2,7-), α,β- (1,3-, 1,6-, and 1,7-), and α,α- (1,4- and 1,5-). Th

Shape-selective synthesis of 2,6-diisopropylnaphthalene on H-mordenite catalysts

Brzozowski, Robert,Buijs, Wim

experimental part, p. 181 - 187 (2012/10/07)

To finally dispel any doubts on the shape-selective formation of 2,6-diisopropylnaphthalene (2,6-DIPN) over H-MOR zeolites, naphthalene alkylation was carried out over high-silica H-MOR catalysts with propylene or isopropanol as an alkylating agent and with or without cyclohexane as a solvent. Isomeric composition of DIPN's, determined by one-dimensional GC analysis, was additionally confirmed with advanced two-dimensional GC × GC. Our results proved beyond any doubt shape-selective formation of 2,6-DIPN over these H-MOR catalysts from naphthalene and propylene and without cyclohexane as a solvent. The DIPN mixture contained 60-64% 2,6-DIPN, and the ratio of 2,6-DIPN/2,7-DIPN was in the range 2.5-2.8. We also showed that shape-selective formation of 2,6-DIPN over H-MOR catalyst was depressed by using isopropanol instead of propylene and in the presence of cyclohexane.

The alkylation of naphthalene over one-dimensional fourteen-membered ring zeolites. the influence of zeolite structure and alkylating agent on the selectivity for dialkylnaphthalenes

Sugi, Yoshihiro,Maekawa, Hiroyoshi,Naiki, Hiroaki,Komura, Kenichi,Kubota, Yoshihiro

experimental part, p. 1166 - 1174 (2009/05/06)

The alkylation, i.e., isopropylation, s-butylation, and t-butylation, of naphthalene (NP) was examined over one-dimensional fourteen-membered (14-MR) zeolites: CIT-5 (CF1), UTD-1 (DON), and SSZ-53 (SFH), and compared to the results over H-mordenite (MOR)

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