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1,3-Dioxolane-2-butanenitrile, 2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56881-73-3

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56881-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56881-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,8 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56881-73:
(7*5)+(6*6)+(5*8)+(4*8)+(3*1)+(2*7)+(1*3)=163
163 % 10 = 3
So 56881-73-3 is a valid CAS Registry Number.

56881-73-3SDS

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 4-(2-methyl-1,3-dioxolan-2-yl)butanenitrile

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolane-2-butanenitrile,2-methyl

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:56881-73-3 SDS

56881-73-3Relevant academic research and scientific papers

Method and compounds for diagnosing coronary artery disease

-

, (2008/06/13)

The present invention relates generally to methods of diagnosis, evaluation and treatment of coronary artery disease in mammals using substituted catecholamines and compounds therefore. It also relates to the preparation, use and administration of these compounds which are useful in the diagnosis, evaluation and treatment of coronary artery disease by means of a feedback controlled drug delivery system that delivers exercise simulating agents which are capable of eliciting acute responses similar to those elicited by aerobic exercise.

Total synthesis of antibiotic karnamicin B1

Umemura, Kazuyuki,Watanabe, Koichi,Ono, Kazumasa,Yamaura, Masanori,Yoshimura, Juji

, p. 4811 - 4814 (2007/10/03)

The novel antifungal karnamicin B1 (1), 5-hydroxy-3,4-dimethoxy-2-{2-(4-oxopentyl)-4-thiazolyl}pyridine-6-carboxamide was first synthesized via the formation of partially methylated trihydroxy pyridine by ring-transformation from the corresponding furan derivative and subsequent regioselective introduction of 2,6-substituents using Meisenheimer-type reaction.

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