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trans-1,2-Di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129662-32-4 Structure
  • Basic information

    1. Product Name: trans-1,2-Di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene-1,2-diol
    2. Synonyms: trans-1,2-Di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene-1,2-diol
    3. CAS NO:129662-32-4
    4. Molecular Formula:
    5. Molecular Weight: 288.341
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129662-32-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: trans-1,2-Di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene-1,2-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-1,2-Di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene-1,2-diol(129662-32-4)
    11. EPA Substance Registry System: trans-1,2-Di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene-1,2-diol(129662-32-4)
  • 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: 129662-32-4(Hazardous Substances Data)

129662-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129662-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,6 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 129662-32:
(8*1)+(7*2)+(6*9)+(5*6)+(4*6)+(3*2)+(2*3)+(1*2)=144
144 % 10 = 4
So 129662-32-4 is a valid CAS Registry Number.

129662-32-4Relevant articles and documents

TOTAL SYNTHESIS OF chiro-INOSITOL 2,3,5-TRISPHOSPHATE: A myo-INOSITOL 1,4,5-TRISPHOSPHATE ANALOGUE FROM BENZENE VIA PHOTO-OXIDATION

Carless, Howard A. J.,Busia, Kofi

, p. 1617 - 1620 (1990)

The inositol tris- and tetrakis-phosphate analogues (4) and (14) have been synthesized from benzene by a sequence including reaction of singlet oxygen with a trans-cyclohexa-3,5-diene-1,2-diol (3) derivative.

Synthesis of racemic 6-deoxy-6-fluoro-chiro-inositol 2,3,5-trisphosphate

Carless,Busia

, p. 207 - 215 (2007/10/02)

The synthesis of (±)-6-deoxy-6-fluoro-chiro-inositol 2,3,5-trisphosphate (4) is reported, starting from cyclohexa-1,4-diene. A key step involved the stereospecific 1,4-addition of singlet oxygen to trans-1,2-di-O-(2-methoxyethoxymethyl)cyclohexa-3,5-diene

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