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17637-70-6

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17637-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17637-70-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,3 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17637-70:
(7*1)+(6*7)+(5*6)+(4*3)+(3*7)+(2*7)+(1*0)=126
126 % 10 = 6
So 17637-70-6 is a valid CAS Registry Number.

17637-70-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-propylium

1.2 Other means of identification

Product number -
Other names Ethylphenylcarbeniumion

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:17637-70-6 SDS

17637-70-6Downstream Products

17637-70-6Relevant articles and documents

Site of Gas-phase Methylation of 1-Phenyl-2-aminopropane

Zappey, Herman,Fokkens, Roel H.,Ingemann, Steen,Nibbering, Nico M. M.,Florencio, Helena

, p. 587 - 594 (2007/10/02)

The regioselectivity of methyl cation transfer from (CH3)2F(1+), (CH3)2Cl(1+) and (CH3)3O(1+) to 1-phenyl-2-aminopropane was studied by Fourier transform ion cyclotron resonance in combination with collision-induced dissociation and neutralization-reionization mass spectrometry of the stable (1+) ions formed in a chemical ionization source.The (CH3)2F(1+) ion transfers a methyl cation to the NH2 group and the phenyl ring with almost equal probability.Predominant CH3(1+) transfer to the NH2 group is observed for the (CH3)2Cl(1+) ion whereas the (CH3)3O(1+) ion reacts almost exclusively at the amino group.The preference for m ethylation at NH2 is discussed in terms of a lower methyl cation affinity of the phenyl ring than of the amino group and the existence of an energy barrier for methylation of the phenyl moiety.

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