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2013537-81-8

1αH,5αH-guaia-6-ene-4β,10β-diol is a naturally occurring chemical compound that belongs to the class of guaiane sesquiterpenoids. It is a diol compound, characterized by the presence of two hydroxyl (OH) groups. The prefix "1αH,5αH" denotes the relative stereochemistry of the hydrogen atoms at the 1st and 5th carbon positions of the molecule. The structure of 1αH,5αH-guaia-6-ene-4β,10β-diol features a guaia-6-ene backbone with hydroxyl groups at the 4th and 10th positions, as indicated by the "6-ene-4β,10β-diol" portion of the name. 1αH,5αH-guaia-6-ene-4β,10β-diol exhibits potential biological activities and may find applications in various industries, including medicine, fragrance, and flavor.

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  • 2013537-81-8 Structure

  • Basic information

    1. Product Name: 1αH,5αH-guaia-6-ene-4β,10β-diol
    2. Synonyms: 1αH,5αH-guaia-6-ene-4β,10β-diol
    3. CAS NO:2013537-81-8
    4. Molecular Formula: C15H26O2
    5. Molecular Weight: 238.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2013537-81-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 343.2±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.024±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.78±0.60(Predicted)
    10. CAS DataBase Reference: 1αH,5αH-guaia-6-ene-4β,10β-diol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1αH,5αH-guaia-6-ene-4β,10β-diol(2013537-81-8)
    12. EPA Substance Registry System: 1αH,5αH-guaia-6-ene-4β,10β-diol(2013537-81-8)

  • 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: 2013537-81-8(Hazardous Substances Data)

2013537-81-8 Usage

Uses

Used in Pharmaceutical Industry:
1αH,5αH-guaia-6-ene-4β,10β-diol is used as a pharmaceutical compound for its potential biological activities. The presence of hydroxyl groups and the unique guaiane sesquiterpenoid structure may contribute to its therapeutic properties, making it a candidate for the development of new drugs or as a component in existing formulations.
Used in Fragrance Industry:
1αH,5αH-guaia-6-ene-4β,10β-diol is used as a fragrance ingredient due to its unique scent profile. 1αH,5αH-guaia-6-ene-4β,10β-diol's molecular structure may impart distinct olfactory characteristics, making it valuable in the creation of perfumes, colognes, and other scented products.
Used in Flavor Industry:
1αH,5αH-guaia-6-ene-4β,10β-diol is used as a flavoring agent in the food and beverage industry. Its chemical composition may contribute to the taste and aroma of various products, enhancing the overall sensory experience for consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 2013537-81-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,0,1,3,5,3 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2013537-81:
(9*2)+(8*0)+(7*1)+(6*3)+(5*5)+(4*3)+(3*7)+(2*8)+(1*1)=118
118 % 10 = 8
So 2013537-81-8 is a valid CAS Registry Number.

2013537-81-8Downstream Products

2013537-81-8Relevant articles and documents

Syntheses of (+)-alismoxide and (+)-4-epi-alismoxide

Blay, Gonzalo,Garcia, Begona,Molina, Eva,Pedro, Jose R.

, p. 7866 - 7869 (2007/10/03)

(Chemical Equation Presented) The first total syntheses of (+)-alismoxide and (+)-4-epialismoxide are reported. Formal chemo-, regio-, and stereo-selective addition of water to 10α-acetoxy-1αH,5βH- guaia-3,6-diene afforded the target compounds after reduc

Guaiane-type sesquiterpenoids from Alisma orientalis

Peng, Guo-Ping,Tian, Gang,Huang, Xian-Feng,Lou, Feng-Chang

, p. 877 - 881 (2007/10/03)

Two guaiane-type sesquiterpenoids named orientalol E (1) and orientalol F (3) were isolated from the rhizome of Alisma orientalis (SAM) JUZEP together with two known guaiane-type sesquiterpenoids alismol (2) and alismoxide (4). Their relative stereo-struc

Marine Natural Products. IV. Chemical Constituents of an Okinawan Soft Coral of Xenia sp. (Xeniidae)

Kitagawa, Isao,Kobayashi, Motomasa,Cui, Zheng,Kiyota, Yutaka,Ohnishi, Mayumi

, p. 4590 - 4596 (2007/10/02)

Four new polyhydroxysterols, named xeniasterol-a (4), xeniasterol-b (5), xeniasterol-c (6), and xeniasterol-d (7), were isolated from an Okinawan soft coral of Xenia sp. (Xeniidae).On the basis of chemical and physicochemical evidence, the structures of xeniasterol-a, -b, -c, and -d have been elucidated respectively as 7-O-acetylergost-22E-ene-3β,5α,6β,7β-tetraol (4), 7-O-acetylergosta-3β,5α,6β,7β-tetraol (5), gorgosta-3β,5α,6β-triol (6), and 7-O-acetylgorgosta-3β,5α,6β,7β-tetraol (7).Germacrene-c (1) was also isolated from the same soft coral together with two guaiane-type compounds (2,3), and it has been shown that germacrene-c (1) is readily air-oxidized to yield these cyclization products (2,3).Keywords-soft coral; Xenia sp.; Xeniidae; sterol polyhydroxylated; xeniasterol-a; xeniasterol-b; xeniasterol-c; xeniasterol-d; sesquiterpene; germacrene-c

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