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1070894-12-0

(4S,5S,6R)-2-iodo-4,5,6-tris(methoxymethoxy)cyclohex-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1070894-12-0 Structure

  • Basic information

    1. Product Name: (4S,5S,6R)-2-iodo-4,5,6-tris(methoxymethoxy)cyclohex-2-en-1-one
    2. Synonyms: (4S,5S,6R)-2-iodo-4,5,6-tris(methoxymethoxy)cyclohex-2-en-1-one
    3. CAS NO:1070894-12-0
    4. Molecular Formula:
    5. Molecular Weight: 402.183
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1070894-12-0.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: (4S,5S,6R)-2-iodo-4,5,6-tris(methoxymethoxy)cyclohex-2-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5S,6R)-2-iodo-4,5,6-tris(methoxymethoxy)cyclohex-2-en-1-one(1070894-12-0)
    11. EPA Substance Registry System: (4S,5S,6R)-2-iodo-4,5,6-tris(methoxymethoxy)cyclohex-2-en-1-one(1070894-12-0)

  • 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: 1070894-12-0(Hazardous Substances Data)

1070894-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1070894-12-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,0,8,9 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1070894-12:
(9*1)+(8*0)+(7*7)+(6*0)+(5*8)+(4*9)+(3*4)+(2*1)+(1*2)=150
150 % 10 = 0
So 1070894-12-0 is a valid CAS Registry Number.

1070894-12-0Relevant articles and documents

A Suzuki cross-coupling and intramolecular aza-Michael addition reaction sequence towards the synthesis of 1,10b-epi-7-deoxypancratistatins and their cytotoxicity studies

Pandey, Ganesh,Balakrishnan, Madhesan,Swaroop, Pandrangi Siva

, p. 5839 - 5847 (2008)

The development of an efficient approach to the construction of a phenanthridone is described. The convergent strategy commences with the preparation of Suzuki cross-coupling reaction precursors, arylboronic acid 12 and α-iodo enone 19, from piperonylamine (9) and (-)-D-quinic acid (10), respectively. The coupling of 12 and 19 followed by a key intramolecular aza-Michael addition produced phenanthridone 21 featuring a cis-fused B-C ring junction. The syntheses of compounds 25 and 26, both of which are C-1 and C-10b epimers of the naturally occurring potent antitumor agent 7-deoxypancratistatin (2), from 21 are elaborated in detail in this paper. The cytotoxicities of 25 and 26 were evaluated against three different cancer cell lines. Compound 26 served as a moderate growth inhibitor of THP-1 monocytic cells (GI50 = 14.5 μg/mL). Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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