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25388-20-9

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25388-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25388-20-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,8 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25388-20:
(7*2)+(6*5)+(5*3)+(4*8)+(3*8)+(2*2)+(1*0)=119
119 % 10 = 9
So 25388-20-9 is a valid CAS Registry Number.

25388-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-4-phenylisoxazole

1.2 Other means of identification

Product number -
Other names 3-methyl-4-phenyl-isoxazole

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:25388-20-9 SDS

25388-20-9Relevant articles and documents

Synthesis and reactions of 4-tributylstannyl-3-methylisoxazole

Uchiyama, Daishi,Yabe, Makoto,Kameyama, Hiroshi,Sakamoto, Takao,Kondo, Yoshinori,Yamanaka, Hiroshi

, p. 1301 - 1304 (1996)

1,3-Dipolar cycloaddition reaction of bis(tributylstannyl)acetylene with nitrile oxides, followed by treatment with aqueous ammonia in ethanol in a sealed tube gave 4-tributylstannyl-3-methylisoxazole. The palladium catalyzed cross coupling reaction of the isoxazole with 2-iodonitrobenzene, followed by reductive cyclization afforded 3-acetylindole.

Regioselective conversion of alkynes to 4-substituted and 3,4-disubstituted isoxazoles using titanium-catalyzed multicomponent coupling reactions

Dissanayake, Amila A.,Odom, Aaron L.

experimental part, p. 807 - 812 (2012/01/31)

Conditions have been developed for the regioselective synthesis of 4-substituted isoxazoles from terminal alkynes and 3,4-disubstituted isoxazoles from internal alkynes. The methodology involves a one-pot titanium-catalyzed multicomponent coupling reactio

REGIOSELECTIVE CYCLOADDITION REACTIONS OF ALLYLSILANES AND SILYL ENOL ETHERS WITH NITRONES AND NITRILE OXIDES. SYNTHESIS OF HOMOALLYLAMINES

Hosomi, Akira,Shoji, Hiroaki,Sakurai, Hideki

, p. 1049 - 1052 (2007/10/02)

Allylsilanes and silyl enol ethers add to nitrones and nitrile oxides regioselectively to give the corresponding isoxazolidines and isoxazolines in good yield.Hydrogenative cleavage of the N-O bond of cycloadducts with allylsilanes affords homoallyl

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