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1,3-Benzenedicarboxaldehyde, 2,4,6-trihydroxy-5-(3-methyl-1-oxobutyl)- is a complex organic compound with the molecular formula C14H14O8. It is a derivative of benzene with two carboxylic acid groups (-COOH) at the 1 and 3 positions, and three hydroxyl groups (-OH) at the 2, 4, and 6 positions. Additionally, it features a 3-methyl-1-oxobutyl group attached to the 5 position, which is a four-carbon chain with a methyl group (-CH3) and a carbonyl group (C=O). 1,3-Benzenedicarboxaldehyde,2,4,6-trihydroxy-5-(3-methyl-1-oxobutyl)- is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and functional groups.

96573-43-2

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96573-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96573-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,7 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 96573-43:
(7*9)+(6*6)+(5*5)+(4*7)+(3*3)+(2*4)+(1*3)=172
172 % 10 = 2
So 96573-43-2 is a valid CAS Registry Number.

96573-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name jensenone

1.2 Other means of identification

Product number -
Other names 2,4,6-Trihydroxy-5-(3-methyl-butyryl)-benzene-1,3-dicarbaldehyde

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:96573-43-2 SDS

96573-43-2Relevant academic research and scientific papers

A two-step biomimetic synthesis of antimalarial robustadials A and B

Bharate, Sandip B.,Singh, Inder Pal

, p. 7021 - 7024 (2007/10/03)

The antimalarial robustadials A and B have been synthesized in two steps starting from commercially available phloroglucinol comprising a key biomimetic three-component reaction that involves in situ generation of an o-quinone methide via Knoevenagel cond

An efficient two-step synthesis of jensenone isolated from Eucalyptus jensenii. Synthesis of analogues and evaluation as antioxidants

Bharate, Sandip B.,Chauthe, Siddheshwar K.,Bhutani, Kamlesh K.,Singh, Inder P.

, p. 551 - 555 (2007/10/03)

A phloroglucinol derivative, jensenone (1) isolated from leaves of Eucalyptus jensenii has been synthesized for the first time through a short and efficient two-step procedure starting from commercially available phloroglucinol. The methodology provides a simplified route to introduce diformyl moiety for synthesis of biologically active formylated phloroglucinol compounds such as antimalarial robustadials, cancer chemopreventive euglobals, and antifouling sideroxylonals. Several analogues of jensenone have also been synthesized and evaluated for antioxidant capacity. CSIRO 2005.

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