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(S)-3-Benzyloxy-2-methyl-pentanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 84736-40-3 Structure
  • Basic information

    1. Product Name: (S)-3-Benzyloxy-2-methyl-pentanal
    2. Synonyms:
    3. CAS NO:84736-40-3
    4. Molecular Formula:
    5. Molecular Weight: 206.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84736-40-3.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: (S)-3-Benzyloxy-2-methyl-pentanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-Benzyloxy-2-methyl-pentanal(84736-40-3)
    11. EPA Substance Registry System: (S)-3-Benzyloxy-2-methyl-pentanal(84736-40-3)
  • 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: 84736-40-3(Hazardous Substances Data)

84736-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84736-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,3 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84736-40:
(7*8)+(6*4)+(5*7)+(4*3)+(3*6)+(2*4)+(1*0)=153
153 % 10 = 3
So 84736-40-3 is a valid CAS Registry Number.

84736-40-3Relevant articles and documents

SYNTHESIS OF ALL FOUR POSSIBLE ENANTIOMERS OF SITOPHILATE AGGREGATION PHEROMONE OF THE GRANARY WEEVIL

Cheskis, B. A.,Shpiro, N. A.,Moiseenkov, A. M.

, p. 2205 - 2211 (2007/10/02)

An efficient synthesis of the 3-pentyl ester of 2S-methyl-3R-hydroxypentanoic acid (sitophilate) and its 2S,3S-, 2R,3R-, and 2R,3S-isomers has been carried out starting from the available 2R-methyl-3-butenyl acetate as sole monochiral precursor.

DIASTEREOSELECTION IN 1,3-O- TO -C-ALKYL MIGRATION REACTION OF 1-ALKENYL ALKYL ACETALS CATALYZED BY BORON TRIFLUORIDE ETHERATE

Takahashi, Mitsuru,Suzuki, Hiroharu,Moro-Oka, Yoshihiko,Ikawa, Tsuneo

, p. 4031 - 4034 (2007/10/02)

Remarkable diastereoselection, with (E)-alkenyl alkyl acetal giving selectively the erythro α-alkyl-β-alkoxyaldehyde, and (Z)-acetal leading preferentially to the threo isomer, is observed in the 1,3-O- to -C-alkyl migration reaction of 1-alkenyl alkyl ac

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