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68776-59-0

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68776-59-0 Usage

General Description

5-cyanoisoxazole is a chemical compound with the molecular formula C4H3N3O. It is a heterocyclic molecule containing both nitrogen and oxygen atoms as part of its five-membered ring structure. 5-cyanoisoxazole is used in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and ability to form bonds with other molecular groups. 5-cyanoisoxazole has a variety of applications in the field of organic chemistry and is also used as an intermediate in the production of other complex organic compounds. Furthermore, 5-cyanoisoxazole has potential use in medicinal chemistry and drug discovery due to its unique molecular structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 68776-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,7,7 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68776-59:
(7*6)+(6*8)+(5*7)+(4*7)+(3*6)+(2*5)+(1*9)=190
190 % 10 = 0
So 68776-59-0 is a valid CAS Registry Number.

68776-59-0SDS

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 1,2-oxazole-5-carbonitrile

1.2 Other means of identification

Product number -
Other names QC-8445

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:68776-59-0 SDS

68776-59-0Upstream product

68776-59-0Downstream Products

68776-59-0Relevant articles and documents

Processes for production of oxadiazoline derivatives

-

, (2008/06/13)

A process as represented by reaction scheme: which permits industrial mass production of Δ2-1,2,4-oxadiazoline derivatives having excellent insecticidal effects or salts thereof in high yield with advantage, [wherein X1is halogeno; R1is optionally substituted alkyl, optionally substituted acyl, or ClCO; R2is (1) halogeno, (2) C1-6haloalkyl, (3) C1-6haloalkoxy, or (4) phenyl optionally substituted with C1-6haloalkyl; A is nitrogen or ═CR3— (wherein R3is Cl or CN); R4is C1-6alkyl or C1-6haloalkyl; n is 0, 1 or 2; and X2is halogeno].

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