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133565-20-5

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133565-20-5 Usage

General Description

1,2,3,10,11,12-hexamethoxy-6,7-dihydroxy-6,7-dimethyldibenzocyclooctadiene is a chemical compound with a complex structure. It is a naturally occurring compound found in certain plants and has been studied for its potential medicinal properties. The compound is classified as a lignan, a type of polyphenolic compound found in plants. It possesses antioxidant and anti-inflammatory properties and has been investigated for its potential use in the treatment of various diseases. The compound's unique chemical structure and biological activities make it a subject of interest for researchers in the fields of natural product chemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 133565-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,6 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133565-20:
(8*1)+(7*3)+(6*3)+(5*5)+(4*6)+(3*5)+(2*2)+(1*0)=115
115 % 10 = 5
So 133565-20-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H32O8/c1-23(25)11-13-9-15(27-3)19(29-5)21(31-7)17(13)18-14(12-24(23,2)26)10-16(28-4)20(30-6)22(18)32-8/h9-10,25-26H,11-12H2,1-8H3

133565-20-5SDS

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 1,2-Hmdddo

1.2 Other means of identification

Product number -
Other names 1,2,3,10,11,12-Hexamethoxy-6,7-dihydroxy-6,7-dimethyldibenzocyclooctadiene

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:133565-20-5 SDS

133565-20-5Upstream product

133565-20-5Downstream Products

133565-20-5Relevant articles and documents

Structure determination of biliary metabolites of schizandrin in rat and dog

Ikeya,Sugama,Tanaka,Wakamatsu,Ono,Takeda,Oyama,Maruno

, p. 121 - 129 (1995)

After oral administration of schizandrin (1) to rat, the bile was collected and treated with β-glucuronidase and arylsulfatase. Eleven metabolites, SZ-M0 (3), SZ-M1 (4), SZ-M2 (5), SZ-M3 (6), SZ-M4 (7), SZ-MS (8), SZ M6 (9), SZ-M7 (10), SZ-M8 (11), SZ-M9 (12) and SZ-M10 (13) were isolated from the bile treated with the enzymes. The bile after oral administration of 1 to dog was collected and treated with enzymes in the same way, and eight metabolites, 3-8, 10 and SZ-MD2 (14) were isolated from the bile treated with enzymes. The structures of these metabolites were determined on the basis of chemical and spectral studies. The major metabolite in the bile of rat was 7 and the major metabolites in the bile of dog were 7 and 14.

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