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113340-14-0

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113340-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113340-14-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,4 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113340-14:
(8*1)+(7*1)+(6*3)+(5*3)+(4*4)+(3*0)+(2*1)+(1*4)=70
70 % 10 = 0
So 113340-14-0 is a valid CAS Registry Number.

113340-14-0SDS

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 cis-4-[(benzyloxycarbonyl)amino]cyclohept-2-enol

1.2 Other means of identification

Product number -
Other names -

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:113340-14-0 SDS

113340-14-0Relevant articles and documents

Synthesis of Physoperuvine (8-Methyl-8-azabicyclooctan-1-ol), Norphysoperuvine and Dehydro-derivates

Justice, David E.,Malpass, John R.

, p. 2559 - 2564 (2007/10/02)

4-Aminocycloheptanones have been synthesized in high yield from cyclohepta-1,3-diene.These compounds exist mainly as the bicyclic tautomers (8-azabicyclooctan-1-ol derivatives; the title compounds) as shown by 13C NMR spectroscopy at low temperatur

A SIMPLE APPROACH TO NORTROPANE AND NORTROP-6-ENE DERIVATES

Bathgate, Antoinette,Malpass, John R.

, p. 5937 - 5940 (2007/10/02)

Intramolecular cyclisation of trans-1-(benzylamino)-4-chlorocycloheptane and hept-2-ene gives the corresponding 8-azabicyclo(3.2.1)octane (nortropane) and -oct-6-ene (nortrop-6-ene) derivatives respectively.Under appropriate conditions, cyclohept-1,3-diene is converted into nortropane in 75percent overall yield.

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