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125318-10-7

4-benzyloxy-2-triethylsilylbutanal N-tert-butylimine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125318-10-7 Structure

  • Basic information

    1. Product Name: 4-benzyloxy-2-triethylsilylbutanal N-tert-butylimine
    2. Synonyms: 4-benzyloxy-2-triethylsilylbutanal N-tert-butylimine
    3. CAS NO:125318-10-7
    4. Molecular Formula:
    5. Molecular Weight: 347.616
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125318-10-7.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: 4-benzyloxy-2-triethylsilylbutanal N-tert-butylimine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-benzyloxy-2-triethylsilylbutanal N-tert-butylimine(125318-10-7)
    11. EPA Substance Registry System: 4-benzyloxy-2-triethylsilylbutanal N-tert-butylimine(125318-10-7)

  • 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: 125318-10-7(Hazardous Substances Data)

125318-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125318-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,3,1 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 125318-10:
(8*1)+(7*2)+(6*5)+(5*3)+(4*1)+(3*8)+(2*1)+(1*0)=97
97 % 10 = 7
So 125318-10-7 is a valid CAS Registry Number.

125318-10-7Relevant articles and documents

Preparation of (2E,4E)-2-(2-benzyloxyethyl)-5-(3-methoxy-4-chlorophenyl) penta-2,4-dienal as a key intermediate in the synthesis of strobilurin B

Popovsky,Stepanov,Grigorieva

, p. 1616 - 1621 (2012)

(2E,4E)-2-(2-Benzyloxyethyl)-5-(4-chloro-3-methoxyphenyl)penta-2,4-dienal was obtained by the condensation of 4-benzyloxybutanal N-tert-butylimine with 4-chloro-3-methoxycinnamic aldehyde with ≥98% configurational purity and 40% yield. When 4-benzyloxy-2-triethylsilylbutanal imine was used, a 7: 3 mixture of the target (2E,4E)-dienal with its (2Z,4E)-isomer was obtained in 60% yield; the latter quantitatively isomerized to the thermodynamically preferable target (2E,4E)-dienal.

SYNTHESE STEREOSELECTIVE D'UNE COMPOSANTE DE LA PHEROMONE SEXUELLE DE "L'ECAILLE ROUGE DE CALIFORNIE" : L'ACETATE D'ISOPROPENYL-6 METHYL-3 DECADIENE-3,9 YLE (3Z,6R)

Baudouy, Rene,Prince, Philippe

, p. 2067 - 2074 (2007/10/02)

The stereospecific elaboration of the trisubstituted double bond of acetate 1, is realized by condensation of an α-silylaldimine with aldehide 5 prepared by regioselective ozonolysis of (+)-limonene.

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