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2',4',6'-trihydroxy-3',5'-di-C-β-D-glucopyranosyldihydrochalcone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1235289-00-5

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1235289-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1235289-00-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,2,8 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1235289-00:
(9*1)+(8*2)+(7*3)+(6*5)+(5*2)+(4*8)+(3*9)+(2*0)+(1*0)=145
145 % 10 = 5
So 1235289-00-5 is a valid CAS Registry Number.

1235289-00-5Downstream Products

1235289-00-5Relevant academic research and scientific papers

Quinoid dihydrochalcone dicarbonyl glycoside compound with glucose on A ring, preparation method and neuroprotective activity thereof

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Paragraph 0057-0058; 0063-0066, (2020/09/23)

The invention discloses a class of quinoid dihydrochalcone C-glycoside compounds with glucose on a ring A, a preparation method and anti-cerebral ischemia injury activity thereof, wherein the compoundhas a structure represented by a general formula (I). The preparation method of the compound comprises the following steps: (1) synthesizing a 2,4,6-trihydroxy dihydrochalcone compound; (2) synthesizing a 2,4,6-trihydroxy-3,5-diglucosyl dihydrochalcone C-glycoside compound; and (6) synthesizing a class of quinoid dihydrochalcone C-glycoside compound with glucose in the A ring. The compound disclosed by the invention is simple in preparation method and has a remarkable effect of resisting cerebral ischemia injury.

Base-catalyzed oxidative dearomatization of multisubstituted phloroglucinols: An easy access to C-glucosyl 3,5,6-trihydroxycyclohexa-2,4-dienone derivatives

Gao, Wan,Chen,Yang,Jiang, Jianshuang,Feng, Ziming,Zhang, Xu,Yuan,Zhang, Peicheng

, (2019/08/20)

An efficient and simple method for the protecting group-free synthesis of C-glucosyl 3,5,6-trihydroxycyclohexa-2,4-dienone has been firstly established. This method is compatible with various functional groups, such as benzyl and phenethyl groups, affording a range of C-glucosyl 3,5,6-trihydroxycyclohexa-2,4-dienone derivatives.

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