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94815-32-4

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94815-32-4 Usage

Classification

Isoxazole

Functional Groups

Contains a hydroxyl group (OH)

Application

Commonly used as a building block in the synthesis of pharmaceuticals and other organic chemicals

Utility

Valuable intermediate in the production of various drugs and compounds with biological activity

Safety Considerations

Requires careful handling and proper disposal practices due to potential health hazards and environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 94815-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,1 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94815-32:
(7*9)+(6*4)+(5*8)+(4*1)+(3*5)+(2*3)+(1*2)=154
154 % 10 = 4
So 94815-32-4 is a valid CAS Registry Number.

94815-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-Isobutyl-isoxazol-3-yl)-ethanol

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:94815-32-4 SDS

94815-32-4Downstream Products

94815-32-4Relevant articles and documents

ETHYL 5-SUBSTITUTED-3-ISOXAZOLECARBOXYLATES AS STARTING MATERIALS FOR A CONVENIENT ROUTE TO 3(2H)FURANONES AND 3(2H)IMINOFURANES.

Baraldi, Pier Giovanni,Barco, Achille,Benetti, Simonetta,Manfredini, Stefano,Pollini, Gian Piero,Simoni, Daniele

, p. 4313 - 4316 (2007/10/02)

Cyclodehydration of γ-hydroxy-β-enaminoketones derived from 5-substituted-3-isoxazolemethanols leads to 3(2H)furanones or 3(2H)iminofuranes depending on the substitution pattern and on the reaction conditions.

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