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CAS

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104900-68-7

5-[[(1R,8aα)-Decahydro-1β,2β,4aβ-trimethyl-5-methylenenaphthalene-1α-yl]methyl]-3,4-dihydroxybenzoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 5-[[(1R,8aα)-Decahydro-1β,2β,4aβ-trimethyl-5-methylenenaphthalene-1α-yl]methyl]-3,4-dihydroxybenzoic acid methyl ester

    Cas No: 104900-68-7

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  • 104900-68-7 Structure

  • Basic information

    1. Product Name: 5-[[(1R,8aα)-Decahydro-1β,2β,4aβ-trimethyl-5-methylenenaphthalene-1α-yl]methyl]-3,4-dihydroxybenzoic acid methyl ester
    2. Synonyms: 3-[[(1R,8aα)-Decahydro-1β,2β,4aβ-trimethyl-5-methylenenaphthalen-1α-yl]methyl]-4,5-dihydroxybenzoic acid methyl ester;5-[[(1R,8aα)-Decahydro-1β,2β,4aβ-trimethyl-5-methylenenaphthalene-1α-yl]methyl]-3,4-dihydroxybenzoic acid methyl ester;Dictyoceratin A
    3. CAS NO:104900-68-7
    4. Molecular Formula: C23H32O4
    5. Molecular Weight: 372.49778
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104900-68-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-[[(1R,8aα)-Decahydro-1β,2β,4aβ-trimethyl-5-methylenenaphthalene-1α-yl]methyl]-3,4-dihydroxybenzoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-[[(1R,8aα)-Decahydro-1β,2β,4aβ-trimethyl-5-methylenenaphthalene-1α-yl]methyl]-3,4-dihydroxybenzoic acid methyl ester(104900-68-7)
    11. EPA Substance Registry System: 5-[[(1R,8aα)-Decahydro-1β,2β,4aβ-trimethyl-5-methylenenaphthalene-1α-yl]methyl]-3,4-dihydroxybenzoic acid methyl ester(104900-68-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 104900-68-7(Hazardous Substances Data)

104900-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104900-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,0 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104900-68:
(8*1)+(7*0)+(6*4)+(5*9)+(4*0)+(3*0)+(2*6)+(1*8)=97
97 % 10 = 7
So 104900-68-7 is a valid CAS Registry Number.

104900-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-smenospondiol

1.2 Other means of identification

Product number -
Other names dictyoceratin-A

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:104900-68-7 SDS

104900-68-7Downstream Products

104900-68-7Relevant articles and documents

Total synthesis of (±)-smenospondiol by titanium(III)-mediated tandem radical cyclization

Haruo,Hasegawa,Tanaka,Takahashi

, p. 1935 - 1937 (2001)

We describe the total synthesis of (±)-smenospondiol(1). Stereoselective construction of the drimane skeleton was accomplished by titanium(III)-mediated tandem radical cyclization of epoxide 9. Non-polar solvent is essential for the success of the tandem

Enantioselective synthesis of dictyoceratin-A (smenospondiol) and -C, hypoxia-selective growth inhibitors from marine sponge

Sumii, Yuji,Kotoku, Naoyuki,Fukuda, Akinori,Kawachi, Takashi,Sumii, Yuta,Arai, Masayoshi,Kobayashi, Motomasa

, p. 966 - 975 (2015/03/04)

Total syntheses of (+)-dictyoceratin-C (1) and (+)-dictyoceratin-A (smenospondiol) (2), hypoxia-selective growth inhibitors isolated from marine sponge, were executed. The absolute stereochemistry of the each compound was determined through the enantiosel

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