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3-methoxymethoxy-2-(4-oxo-4,5,6,7-tetrahydro-benzo[d]isoxazol-3-yl)-benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

577975-37-2

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577975-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 577975-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,7,9,7 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 577975-37:
(8*5)+(7*7)+(6*7)+(5*9)+(4*7)+(3*5)+(2*3)+(1*7)=232
232 % 10 = 2
So 577975-37-2 is a valid CAS Registry Number.

577975-37-2SDS

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 3-(methoxymethoxy)-2-(4-oxo-4,5,6,7-tetrahydrobenzo[d]isoxazol-3-yl)benzaldehyde

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:577975-37-2 SDS

577975-37-2Relevant academic research and scientific papers

Catalytic intramolecular crossed aldehyde-ketone benzoin reactions: A novel synthesis of functionalized preanthraquinones

Hachisu, Yoshifumi,Bode, Jeffrey W.,Suzuki, Keisuke

, p. 8432 - 8433 (2003)

Stereochemically and functionally rich polycyclic compounds are obtained by the first crossed aldehyde-ketone benzoin reaction in excellent yield under mild reaction conditions (5-20 mol % thiazolium salt, 10-70 mol % DBU, tBuOH, 40°C, 30 min). This novel catalytic methodology offers a convenient approach to sophisticated molecular architectures useful for the stereocontrolled construction of polycyclic compounds as well as the fully regiocontrolled synthesis of anthra- and naphthoquinones. Copyright

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