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  • 90410-01-8 Structure
  • Basic information

    1. Product Name: cerin
    2. Synonyms:
    3. CAS NO:90410-01-8
    4. Molecular Formula:
    5. Molecular Weight: 442.726
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90410-01-8.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: cerin(CAS DataBase Reference)
    10. NIST Chemistry Reference: cerin(90410-01-8)
    11. EPA Substance Registry System: cerin(90410-01-8)
  • 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: 90410-01-8(Hazardous Substances Data)

90410-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90410-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,1 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90410-01:
(7*9)+(6*0)+(5*4)+(4*1)+(3*0)+(2*0)+(1*1)=88
88 % 10 = 8
So 90410-01-8 is a valid CAS Registry Number.

90410-01-8Relevant articles and documents

Synthetic secofriedelane and friedelane derivatives as inhibitors of human lymphocyte proliferation and growth of human cancer cell lines in vitro

Moiteiro,Justino,Tavares,Marcelo-Curto,Florencio,Nascimento,Pedro,Cerqueira,Pinto

, p. 1273 - 1277 (2001)

Controlled silylation of friedelin (1) from cork smoker wash solids, a byproduct generated during processing of corkboard by steam baking, gave 3-trimethylsiloxyfriedel-2-ene (3) in high yields. Oxidation of 3 with OsO4/NMMO produced 2α-hydroxyfriedelan-3-one (cerin) (5), from which the new 2,3-secofriedelan-2-al-3-oic acid (6) was obtained quantitatively by periodic acid oxidation. Oxidation of 3 with DDQ afforded friedel-1-en-3-one (8). Reductive ozonolysis of 3 gave 2α,3β-dihydroxyfriedelane, pachysandiol A (7). Compound 6 proved to be a potent inhibitor of human lymphocyte proliferation (IC50 = 10.7 μM) and of the growth of a human cancer cell line (GI50 = 5.4-17.2 μM). 13C NMR data for compounds (3, 4, 5, 6a, 7, and 8) are described for the first time.

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