Cas 78876-38-7,Acetic acid 7-(3,4-dimethoxy-phenyl)-10-(3-hydroxy-3-methyl-butyl)-2,2-dimethyl-6-oxo-2H,6H-pyrano[3,2-g]chromen-5-yl ester

78876-38-7

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Basic information

Product Name: Acetic acid 7-(3,4-dimethoxy-phenyl)-10-(3-hydroxy-3-methyl-butyl)-2,2-dimethyl-6-oxo-2H,6H-pyrano[3,2-g]chromen-5-yl ester
Synonyms:
CAS NO:78876-38-7
Molecular Formula:
Molecular Weight: 508.568
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Acetic acid 7-(3,4-dimethoxy-phenyl)-10-(3-hydroxy-3-methyl-butyl)-2,2-dimethyl-6-oxo-2H,6H-pyrano[3,2-g]chromen-5-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid 7-(3,4-dimethoxy-phenyl)-10-(3-hydroxy-3-methyl-butyl)-2,2-dimethyl-6-oxo-2H,6H-pyrano[3,2-g]chromen-5-yl ester(78876-38-7)
EPA Substance Registry System: Acetic acid 7-(3,4-dimethoxy-phenyl)-10-(3-hydroxy-3-methyl-butyl)-2,2-dimethyl-6-oxo-2H,6H-pyrano[3,2-g]chromen-5-yl ester(78876-38-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 78876-38-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78876-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,7 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78876-38:
(7*7)+(6*8)+(5*8)+(4*7)+(3*6)+(2*3)+(1*8)=197
197 % 10 = 7
So 78876-38-7 is a valid CAS Registry Number.

78876-38-7Upstream product

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78876-38-7Relevant academic research and scientific papers

NEW PRENYLATED ISOFLAVONES FROM MILLETTIA PACHYCARPA

Singhal, Ashok K.,Sharma, Ram P.,Madhusudanan, K. P.,Thyagarajan, Gopalakrishna,Herz, Werner,Govindan, Serengolam V.

, p. 803 - 806 (1981)

Isolation of four new isoflavones from a new collection of Millettia pachycarpa is reported.Proof of the structure of lupinifolol, previously isolated from M. pachycarpa, by synthesis of dehydrolupinifolol is described.Key Word Index- Millettia pachycarpa; Leguminosae; Lotodoideae; prenylated isoflavones.

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