Cas 956222-36-9,4-(2-{4-[2-(4-chlorophenyl)-2H-tetrazol-5-yl]-3-methoxyphenoxy}ethyl)morpholine

956222-36-9

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Basic information

Product Name: 4-(2-{4-[2-(4-chlorophenyl)-2H-tetrazol-5-yl]-3-methoxyphenoxy}ethyl)morpholine
Synonyms: 4-(2-{4-[2-(4-chlorophenyl)-2H-tetrazol-5-yl]-3-methoxyphenoxy}ethyl)morpholine
CAS NO:956222-36-9
Molecular Formula:
Molecular Weight: 415.879
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-(2-{4-[2-(4-chlorophenyl)-2H-tetrazol-5-yl]-3-methoxyphenoxy}ethyl)morpholine(CAS DataBase Reference)
NIST Chemistry Reference: 4-(2-{4-[2-(4-chlorophenyl)-2H-tetrazol-5-yl]-3-methoxyphenoxy}ethyl)morpholine(956222-36-9)
EPA Substance Registry System: 4-(2-{4-[2-(4-chlorophenyl)-2H-tetrazol-5-yl]-3-methoxyphenoxy}ethyl)morpholine(956222-36-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 956222-36-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 956222-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,2,2 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 956222-36:
(8*9)+(7*5)+(6*6)+(5*2)+(4*2)+(3*2)+(2*3)+(1*6)=179
179 % 10 = 9
So 956222-36-9 is a valid CAS Registry Number.

956222-36-9Upstream product

956222-36-9Downstream Products

956222-37-0 4-(2-{4-[2-(4-chlorophenyl)-2H-tetrazol-5-yl]-3-isopropoxyphenoxy}ethyl)morpholine

956222-36-9Relevant academic research and scientific papers

Convenient synthesis of highly functionalized pyrazolines via mild, photoactivated 1,3-dipolar cycloaddition

Wang, Yizhong,Rivera Vera, Claudia I.,Lin, Qing

, p. 4155 - 4158 (2008/02/12)

A mild, photoactivated 1,3-dipolar cycloaddition procedure was successfully developed for the synthesis of polysubstituted pyrazolines. This procedure involved the in situ generation of the reactive nitrile imine dipoles using a hand-held UV lamp at 302 n

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