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2001-50-5

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2001-50-5 Usage

Also known as

O-hydrogenated naphthalene

Physical state

Colorless liquid

Odor

Mild, aromatic

Solubility

Insoluble in water

Primary uses

Solvent for chemical processes
Production of polymers, resins, and dyes
Reaction medium in organic synthesis
Lubricant additive

Toxicity

Low acute toxicity

Carcinogenicity

Not known to be carcinogenic

Mutagenicity

Not known to be mutagenic

Reproductive toxicity

Not known to be toxic to reproduction

Health hazards

Can cause irritation to eyes, skin, and respiratory system at high levels

Safety precautions

Handle and store in a well-ventilated area, use appropriate personal protective equipment

Check Digit Verification of cas no

The CAS Registry Mumber 2001-50-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,0 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2001-50:
(6*2)+(5*0)+(4*0)+(3*1)+(2*5)+(1*0)=25
25 % 10 = 5
So 2001-50-5 is a valid CAS Registry Number.

2001-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,4aα,5,8,8aβ-Octahydronaphthalene

1.2 Other means of identification

Product number -
Other names trans-octalin

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:2001-50-5 SDS

2001-50-5Relevant articles and documents

Synthesis of poly(decahydro-2-naphthyl methacrylate)s with different geometric structures and effects of side-group dynamics on polymer properties investigated by thermal and dynamic mechanical analyses and DFT calculations

Ozaki, Anri,Sumita, Koha,Goto, Kunihiro,Matsumoto, Akikazu

, p. 2941 - 2950 (2013/06/05)

We prepared the geometric isomers of decahydro-2-naphthols as the source materials for the synthesis of poly(decahydro-2-naphthyl methacrylate)s [poly(DNMA)-I, -II, -III, and -IV] including alicyclic ester groups with different geometric structures. The geometry and conformational dynamics of the decahydro-2-naphthyl moieties were investigated by NMR spectroscopy and DFT calculations. We synthesized each isomer of the methacrylic monomers, polymerized them, and investigated the optical, thermal, and mechanical properties of poly(DNMA)s with different isomer compositions. The Tg values of the poly(DNMA)s were in the following order: 139.3 C for poly(DNMA)-II 3/g, 1.489, and 42-44, respectively.

Diels-Alder Reactions of Cycloalkenones. 12. Reaction of trans-Δ1,2-3-Octalone with (E)-Piperylene

Angell, E. Charles,Fringuelli, Francesco,Pizzo, Ferdinando,Taticchi, Aldo,Wenkert, Ernest

, p. 1424 - 1426 (2007/10/02)

The Diels-Alder reaction of (E)-piperylene with trans-Δ1,2-3-octalone under aluminum chloride catalysis is described and structure analysis of the adducts by NMR spectroscopy is presented.The diastereofacial selectivity of the reaction is discu

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