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7335-04-8

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7335-04-8 Usage

Physical state

Colorless liquid

Uses

Precursor in the synthesis of various pharmaceuticals and organic compounds, potential neuroprotective agent, effects on the central nervous system, synthesis of heterocyclic compounds, building block in organic chemistry

Stability

Stable under normal conditions

Handling precautions

Can be handled safely with proper precautions

Importance

Wide range of potential applications in research and industry

Check Digit Verification of cas no

The CAS Registry Mumber 7335-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7335-04:
(6*7)+(5*3)+(4*3)+(3*5)+(2*0)+(1*4)=88
88 % 10 = 8
So 7335-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H19N/c1-4-8-11(9-5-1)10-6-2-3-7-10/h10H,1-9H2

7335-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Cyclopentylpiperidine

1.2 Other means of identification

Product number -
Other names Piperidino-1-cyclopentan

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:7335-04-8 SDS

7335-04-8Downstream Products

7335-04-8Relevant articles and documents

HYDROGENOLYTIC CLEAVAGE OF PYRIDINE ON DIFFERENT COBALT-MOLYBDENUM AND NICKEL-TUNGSTEN CATALYSTS

Cerny, Mirko,Kraus, Milos

, p. 1348 - 1354 (2007/10/02)

Composition of the reaction products formed by hydrogenation of pyridine at 300 deg C and 15 MPa in the presence of 15 sulphided and unsulphided molybdenum and tungsten catalysts promoted by cobalt and by nickel, respectively, using alumina as the support in most cases, has been examined.It has been proved that the catalyst composition affects both its hydrogenation activity and the ratio of transalkylation to cracking (or hydrocracking) reactions.Relations between the catalysts composition and its activity and selectivity found for the reaction of pyridine differ from those reported for hydrogenolytic cleavage of thiophene, hydrogenation and isomerisation of cyclohexene.

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