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3-nitroxypropyl 2-(3-cyanobenzylidene)acetoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

170748-98-8

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170748-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170748-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,7,4 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 170748-98:
(8*1)+(7*7)+(6*0)+(5*7)+(4*4)+(3*8)+(2*9)+(1*8)=158
158 % 10 = 8
So 170748-98-8 is a valid CAS Registry Number.

170748-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitroxypropyl 2-(3-cyanobenzylidene)acetoacetate

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:170748-98-8 SDS

170748-98-8Downstream Products

170748-98-8Relevant academic research and scientific papers

Novel 2-amino-1,4-dihydropyridine calcium antagonists. I. Synthesis and antihypertensive effects of 2-amino-1,4-dihydropyridine derivatives having nitroxyalkoxycarbonyl groups at 3- and/or 5-position

Kobayashi,Inoue,Kita,Yoshiya,Nishino,Oizumi,Kimura

, p. 788 - 796 (2007/10/02)

Novel 2-amino-1,4-dihydropyridine derivatives, which contain nitroxy-alkoxycarbonyl groups at the 3- and/or 5-position, were synthesized and their pharmaceutical effect was evaluated in spontaneously hypertensive rats. The structure-activity relationships are discussed in terms of potency, onset-rapidity, and duration of antihypertensive activity. Remarkably prolonged duration of antihypertensive action was observed when a tertiary amino group was introduced on either side of an ester chain.

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