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13946-02-6

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13946-02-6 Usage

Uses

vasoconstrictor, antihistamine, nasal decongestant

Check Digit Verification of cas no

The CAS Registry Mumber 13946-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,4 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13946-02:
(7*1)+(6*3)+(5*9)+(4*4)+(3*6)+(2*0)+(1*2)=106
106 % 10 = 6
So 13946-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H25N/c1-9(2)7-6-8-11(5)12-10(3)4/h9-12H,6-8H2,1-5H3

13946-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-N-propan-2-ylheptan-2-amine

1.2 Other means of identification

Product number -
Other names N-isopropyl-6-methylheptan-2-amine

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:13946-02-6 SDS

13946-02-6Downstream Products

13946-02-6Relevant articles and documents

Markovnikov vinylborinates from 9-oxa-10-borabicyclo[3.3.2]decanes

Soderquist, John A.,Ramos, Jorge,Matos, Karl

, p. 6639 - 6642 (1997)

Alkylborinates 1 react with α-methoxyvinyllithium (LiAMV) to produce stable 'ate' complexes, 2, which undergo BCl3-induced alkyl group migration providing new air-stable vinylborinates, 3. These intermediates which are readily converted to either unsymmetrical 1,1-disubstituted alkenes (7) via the Suzuki-Miyaura coupling or, oxidatively, to methyl ketones, (8), one of which was converted to the antihistaminic drug, metron S, 10.

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