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CAS

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133210-27-2

(1E,5E)-1-(benzyloxymethyloxy)-2,3-dimethyl-4-hydroxy-1,5-decadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133210-27-2 Structure

  • Basic information

    1. Product Name: (1E,5E)-1-(benzyloxymethyloxy)-2,3-dimethyl-4-hydroxy-1,5-decadiene
    2. Synonyms:
    3. CAS NO:133210-27-2
    4. Molecular Formula:
    5. Molecular Weight: 318.456
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133210-27-2.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: (1E,5E)-1-(benzyloxymethyloxy)-2,3-dimethyl-4-hydroxy-1,5-decadiene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1E,5E)-1-(benzyloxymethyloxy)-2,3-dimethyl-4-hydroxy-1,5-decadiene(133210-27-2)
    11. EPA Substance Registry System: (1E,5E)-1-(benzyloxymethyloxy)-2,3-dimethyl-4-hydroxy-1,5-decadiene(133210-27-2)

  • 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: 133210-27-2(Hazardous Substances Data)

133210-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133210-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,2,1 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133210-27:
(8*1)+(7*3)+(6*3)+(5*2)+(4*1)+(3*0)+(2*2)+(1*7)=72
72 % 10 = 2
So 133210-27-2 is a valid CAS Registry Number.

133210-27-2Downstream Products

133210-27-2Relevant articles and documents

Evidence for synclinal transition state in the reactions of aromatic aldehydes with α-(alkoxy)allylstannanes

Gung, Benjamin W.,Smith, Daniel T.,Wolf, Mark A.

, p. 5455 - 5466 (2007/10/02)

Unlike aliphatic aldehydes, aromatic aldehydes produce greater than 95% of syn-(Z) enol ether when treated with α-(alkoxy)allylstannanes in the presence of BF3·Et2O. However, in the presence of TiCl4, the reaction of p-chloro-o-methoxybenzaldehyde with α-(alkoxy)crotylstannane produced predominantly the syn-(E) isomer.

Remarkable increase in the diastereofacial selectivity of the addition of β-methyl α-(alkoxy)allylstannane to aldehydes: Substituent effects on diastereofacial selectivity

Gung, Benjamin W.,Smith, Daniel T.,Wolf, Mark A.

, p. 13 - 16 (2007/10/02)

Several new chiral allylstannanes were prepared and reacted with aldehydes. Excellent diastereofacial selectivity was observed for the reactions of allylstannane 1 with aldehydes in the presence of BF3·Et2O. This is in contrast to the results from other allylstannanes which do not bear a β-methyl group. These observations were rationalized based on a combination of steric and electronic effects.

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