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  • (1R,4S)-4-(acetyloxy)-4-{(2R,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}-1-{(2S,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}butyl acetate

    Cas No: 134856-96-5

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  • Xi'an Yinherb Bio-Tech Co., Ltd.
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  • (1R,4S)-4-(acetyloxy)-4-{(2R,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}-1-{(2S,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}butyl acetate

    Cas No: 134856-96-5

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  • Chongqing Ihlen Biotechlogy Co.,Ltd
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  • 134856-96-5 Structure
  • Basic information

    1. Product Name: (1R,4S)-4-(acetyloxy)-4-{(2R,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}-1-{(2S,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}butyl acetate
    2. Synonyms: 2,5-furandimethanol, alpha~5~-[(3R)-3-(acetyloxy)-3-[(2S,5R)-tetrahydro-5-[(1S)-1-hydroxy-1,5-dimethyl-4-hexen-1-yl]-2-methyl-2-furanyl]propyl]tetrahydro-alpha~2~,5-dimethyl-alpha~2~-(4-methyl-3-penten-1-yl)-, 5-acetate, (alpha~2~S,alpha~5~S,2R,5R)-
    3. CAS NO:134856-96-5
    4. Molecular Formula: C34H58O8
    5. Molecular Weight: 594.8195
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134856-96-5.mol
    9. Article Data: 3
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 656.7°C at 760 mmHg
    3. Flash Point: 192.8°C
    4. Appearance: N/A
    5. Density: 1.065g/cm3
    6. Vapor Pressure: 4.91E-20mmHg at 25°C
    7. Refractive Index: 1.499
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (1R,4S)-4-(acetyloxy)-4-{(2R,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}-1-{(2S,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}butyl acetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1R,4S)-4-(acetyloxy)-4-{(2R,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}-1-{(2S,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}butyl acetate(134856-96-5)
    12. EPA Substance Registry System: (1R,4S)-4-(acetyloxy)-4-{(2R,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}-1-{(2S,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyltetrahydrofuran-2-yl}butyl acetate(134856-96-5)
  • 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: 134856-96-5(Hazardous Substances Data)

134856-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134856-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,5 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134856-96:
(8*1)+(7*3)+(6*4)+(5*8)+(4*5)+(3*6)+(2*9)+(1*6)=155
155 % 10 = 5
So 134856-96-5 is a valid CAS Registry Number.

134856-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1S,4R)-4-acetyloxy-1-[(2R,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyloxolan-2-yl]-4-[(2S,5R)-5-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-2-methyloxolan-2-yl]butyl] acetate

1.2 Other means of identification

Product number -
Other names ( )-Eurylene

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:134856-96-5 SDS

134856-96-5Upstream product

134856-96-5Downstream Products

134856-96-5Relevant articles and documents

Enantioselective total synthesis of eurylene, 14-deacetyl eurylene, and their 11-epimers: The relation between lonophoric nature and cytotoxicity

Hioki, Hideaki,Yoshio, Suzuyo,Motosue, Masatoshi,Oshita, Yuka,Nakamura, Yukari,Mishima, Daisaku,Fukuyama, Yoshiyasu,Kodama, Mitsuaki,Ueda, Keisuke,Katsu, Takashi

, p. 961 - 964 (2007/10/03)

(Equation presented) Enantioselective synthesis of eurylene, 14-deacetyl eurylene, and their 11-epimers was achieved. The characteristic structural feature of these compounds is two tetrahydrofuran (THF) rings substituted in different stereochemistry. The

Total synthesis of (+)-eurylene

Ujihara, Kazuya,Shirahama, Haruhisa

, p. 2039 - 2042 (2007/10/03)

Eurylene 1, a cytotoxic bicyclic squalenoid isolated from Eurycoma longifola, has been synthesized utilizing the double vanadium(V)-catalyzed oxidation reaction of different bishomoallyl alcohol systems.

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