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13509-75-6

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13509-75-6 Usage

General Description

Benzenemethanamine, also known as N-butyl-N-methylbenzylamine, is a chemical compound with the formula C11H17N. It is an organic compound and a member of the amine class of chemicals, which are known for their distinctive and often unpleasant odor. This particular compound is commonly used as an intermediate or precursor in the synthesis of various pharmaceutical and industrial compounds. Its primary applications include use as a corrosion inhibitor, an antioxidant, and as an ingredient in the production of rubber and plastic materials. It is also used as a stabilizer in the manufacturing of different types of polymers. However, it is important to handle this chemical with care, as it can be harmful if ingested, inhaled, or comes into contact with the skin or eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 13509-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,0 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13509-75:
(7*1)+(6*3)+(5*5)+(4*0)+(3*9)+(2*7)+(1*5)=96
96 % 10 = 6
So 13509-75-6 is a valid CAS Registry Number.

13509-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methyl-1-phenyl-1-pentanamine

1.2 Other means of identification

Product number -
Other names 2-chloro-1-(3-methyl-3-phenylcyclobutyl)ethan-1-one

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:13509-75-6 SDS

13509-75-6Downstream Products

13509-75-6Relevant articles and documents

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Savignac,Leroux

, p. C47,C48 (1973)

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Direct transformation of secondary amides into secondary amines: Triflic anhydride activated reductive alkylation

Xiao, Kai-Jiong,Wang, Ai-E,Huang, Pei-Qiang

supporting information; experimental part, p. 8314 - 8317 (2012/09/08)

Versatile and mild: The first general method for the title transformation has been developed (see scheme; 2-F-Py=2-fluoropyridine; Tf=trifluorosulfonyl). The amines are synthesized in good yields and the ketimine intermediates can be isolated before the r

Triflamides: Elimination of the triflyl anion versus substitution of the trifluoromethide group

Bozec-Ogor,Salou-Guiziou,Yaouanc,Handel

, p. 6063 - 6066 (2007/10/02)

Base-induced elimination of CF3SO2- and nucleophilic substitution of CF3- were observed in the reaction of secondary triflamides with alkyllithium reagents.

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