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Cedrusin, a naturally occurring chemical compound found in the heartwood of cedar trees from the Cedrus genus, is recognized for its unique antioxidant properties. It has been identified as a potential therapeutic agent for a variety of health conditions due to its anti-inflammatory, antimicrobial, and cancer cell growth inhibitory activities, making it a promising bioactive compound with diverse potential health benefits.

75775-36-9

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75775-36-9 Usage

Uses

Used in Pharmaceutical Industry:
Cedrusin is used as an anti-inflammatory agent for its ability to reduce inflammation, which is beneficial in treating inflammatory diseases.
Used in Antimicrobial Applications:
Cedrusin is used as an antimicrobial agent for its capacity to combat infections by inhibiting the growth of various microorganisms, thus proving useful in treating infectious diseases.
Used in Cancer Treatment:
Cedrusin is used as a potential cancer treatment due to its demonstrated ability to inhibit the growth of cancer cells, suggesting its utility in oncology for managing cancer progression.
Used in Nutraceutical Industry:
Considering its antioxidant properties, Cedrusin could be used as a nutraceutical ingredient to support overall health and well-being by combating oxidative stress and promoting cellular health.

Check Digit Verification of cas no

The CAS Registry Mumber 75775-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,7 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75775-36:
(7*7)+(6*5)+(5*7)+(4*7)+(3*5)+(2*3)+(1*6)=169
169 % 10 = 9
So 75775-36-9 is a valid CAS Registry Number.

75775-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-(3-hydr oxypropyl)-2,3-dihydro-1-benzofuran-7-ol

1.2 Other means of identification

Product number -
Other names -

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:75775-36-9 SDS

75775-36-9Relevant articles and documents

Bioactive lignans from the Trunk of Abies holophylla

Kim, Chung Sub,Kwon, Oh Wook,Kim, Sun Yeou,Lee, Kang Ro

, p. 2131 - 2135 (2014/01/06)

Six new lignans (1-6) were isolated from the trunk of Abies holophylla MAXIM, together with 11 known lignans (7-17). The structures of 1-7 were elucidated by spectroscopic methods, acid hydrolysis, and use of the modified Mosher's method. The effects of the isolates on nerve growth factor induction in a C6 rat glioma cell line were evaluated. Compounds 6, 7, and 13 showed significant induction of nerve growth factor secretion at concentrations of 10 μM. Compounds 1, 5, 6, and 16 showed moderate inhibitory effects on nitric oxide production in lipopolysaccharide-activated BV-2 cells (IC50 28.5-36.4 μM).

Studies on the constituents of Clematis species. VI. The constituents of Clematis stans SIEB et ZUCC

Kizu,Shimana,Tomimori

, p. 2187 - 2194 (2007/10/03)

From the roots of Clematis stans three new oleanane-type triterpenoid saponins named clemastanoside A, B and C, and two new lignan glycosides named clemastanin A and B, have been isolated together with three known triterpenoid saponins, huzhangoside B, C and D, and three known lignan glycosides, (+)-lariciresinol 4-O-β-D-glucopyranoside, (+)-lariciresinol 4'- O-β-D-glucopyranoside and (+)-pinoresinol 4,4'-O-bis-β-D-glucopyranoside. In addition, from the leaves, four new oleanane-type triterpenoid saponins, named clemastanoside D, E, F and G, have been isolated together with five known triterpenoid saponins, hederasaponin B, kizutasaponin K12, huzhangoside B, sieboldianoside B and huzhangoside D, and three known flavonoids, isoquercitrin, ratin and quercetin 3-O-β-D-glucuronopyranoside. The structures of the new compounds were elucidated based on chemical and physicochemical evidence as follows: clemastanoside A, 3-O-β-D- ribopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl oleanolic acid 28-O-(4-O-acetyl)-α-L-rhamnopyranosyl-(1→4)-β-D- glucopyranosyl-(1→6)-β-D-glucopyranosyl ester (terminal rhamnosyl 4-O- acetate of huzhangoside B); clemastanoside B and C, 3-O-β-D-xylopyranosyl- and 3-O-β-D-ribopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-β-D- galactopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl-(1→4)-β-D- glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, respectively; clemastanoside D, 3-O-β-D-ribopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L- arabinopyranosyl hederagenin 28-O-β-D-glucopyranosyl ester; clemastanoside E, F and G, terminal rhamnosyl 4-O-, 3-O- and 2-O-acetate of 3-O-β-D- ribopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl hederagenin 28-O-α-L-rhamno-pyranosyl-(1→4)-β-D-glucopyranosyl-(1→6]-β- D-glucopyranosyl ester, respectively; clemastanin A, (7S,8R)-3-methoxy- 3',4,9,9'-tetrahydroxy-4',7-epoxy-5',8-lignan 3'-O-β-D-glucopyranoside; clemastanin B, (+)-lariciresinol 4,4'-O-bis-β-D-glucopyranoside.

PHENOLIC EXTRACTIVES FROM ROOT BARK OF PICEA ABIES

Pan, Hefeng,Lundgren, Lennart N.

, p. 1422 - 1428 (2007/10/02)

Five new compounds, viz., 3,4-dimethoxyphenyl 2-O-(3-O-methyl-α-L-rhamnopyranosyl)-β-D-glucopyranoside, 4'-hydroxyphenacyl β-D-glucopyranoside, (2R,3R)-2,3-dihydro-7-hydroxy-2-(4'-hydroxy-3'-methoxyphenyl)-3-hydroxymethyl-5-benzofuranpropanol 4'-O-(3-O-methyl-α-L-rhamnopyranoside), 1-(4'-hydroxy-3'-methoxyphenyl)-2--1,3-propanediol 4'-O-β-D-xylopyranoside and 3'-O-methylcatechin 7-O-β-D-glucopyranoside, together with several known compounds were isolated from the root bark of Picea abies.The structures were elucidated on the basis of chemical and spectroscopic evidence. - Key words: Picea abies; Pinaceae; root bark; monoaryl glycosides; stilbenes; lignans; flavonoids; proanthocyanidins.

Total Synthesis of Cedrusin and its Methyl Ether

Antus, Sandor,Baitz-Gacs, Eszter,Bauer, Rudolf,Gottsegen, Agnes,Seligmann, Otto,Wagner, Hildebert

, p. 495 - 497 (2007/10/02)

A simple synthesis of the racemates of two naturally occuring neolignans 1 and 2 was achieved starting from caffeic acid ethyl ester and the methyl ferulate 6, respectively.

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