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Benzaldehyde, 2,4,6-trihydroxy-3-(1-oxopropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96573-29-4

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96573-29-4 Usage

Preparation

Preparation by reaction of ethyl orthoformate with phloropropiophenone in methylene chloride in the presence of aluminium chloride cooling in an ice bath for 30 min (70%).

Check Digit Verification of cas no

The CAS Registry Mumber 96573-29-4 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, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96573-29:
(7*9)+(6*6)+(5*5)+(4*7)+(3*3)+(2*2)+(1*9)=174
174 % 10 = 4
So 96573-29-4 is a valid CAS Registry Number.

96573-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-trihydroxy-3-propanoylbenzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2,4,6-trihydroxy-3-(1-oxopropyl)

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:96573-29-4 SDS

96573-29-4Downstream Products

96573-29-4Relevant academic research and scientific papers

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 (2005)

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.

Structure/Activity relationships of Grandinol: a Germination Inhibitor in Eucalyptus

Bolte, Matthew L.,Crow, Wilfrid D.,Takahashi, Nobutaka,Sakurai, Akira,Uji-Ie, Masami,Yoshida, Shigeo

, p. 761 - 768 (2007/10/02)

Structure/activity relationships of grandinol (1), which shows potent inhibition to cress germination, were examined by an activity comparison of many synthetic analogues.The result clearly indicates that a combination of two carbonyl functionalities on a

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