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2-[4-(azepan-1-yl)but-2-yn-1-yl]-1H-isoindole-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19446-29-8

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19446-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19446-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,4 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19446-29:
(7*1)+(6*9)+(5*4)+(4*4)+(3*6)+(2*2)+(1*9)=128
128 % 10 = 8
So 19446-29-8 is a valid CAS Registry Number.

19446-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(azepan-1-yl)but-2-ynyl]isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names Phthalimide,N-(4-(hexahydro-1H-azepin-1-yl)but-2-ynyl)

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:19446-29-8 SDS

19446-29-8Downstream Products

19446-29-8Relevant academic research and scientific papers

Synthesis and biological evaluation of N-(4-t-amino-2-butynyloxy) and N-(4-t-amino-2-butynyl) phthalimides

Eldeen,Shubber,Musa,et al.

, p. 85 - 88 (2007/10/02)

A series of N-(4-t-amino-2-butynyloxy) and N-(4-t-amino-2-butynyl) phthalimides have been prepared through the Mannich reaction from N-(propargyloxy) phthalimide or N-propargylphthalimide with formaldehyde and various cyclic amines. These compounds have been investigated for blockade of oxotremorine in intact mice, and for their antagonistic activity towards acetylcholine on isolated guinea pig ileal preparations. None of the oxyphthalimido derivatives show oxotremorine antagonistic activity, but all have an acetylcholine antagonistic activity. The phthalimido compounds, on the other hand, have both oxotremorine and acetylcholine antagonistic activity.

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