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[C4H2N(2,5-CH2NMe2)2Al(SCPh3)2] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1341127-32-9 Structure
  • Basic information

    1. Product Name: [C4H2N(2,5-CH2NMe2)2Al(SCPh3)2]
    2. Synonyms:
    3. CAS NO:1341127-32-9
    4. Molecular Formula:
    5. Molecular Weight: 758.043
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1341127-32-9.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: [C4H2N(2,5-CH2NMe2)2Al(SCPh3)2](CAS DataBase Reference)
    10. NIST Chemistry Reference: [C4H2N(2,5-CH2NMe2)2Al(SCPh3)2](1341127-32-9)
    11. EPA Substance Registry System: [C4H2N(2,5-CH2NMe2)2Al(SCPh3)2](1341127-32-9)
  • 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: 1341127-32-9(Hazardous Substances Data)

1341127-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1341127-32-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,1,1,2 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1341127-32:
(9*1)+(8*3)+(7*4)+(6*1)+(5*1)+(4*2)+(3*7)+(2*3)+(1*2)=109
109 % 10 = 9
So 1341127-32-9 is a valid CAS Registry Number.

1341127-32-9Downstream Products

1341127-32-9Relevant articles and documents

Synthesis and protonolysis of neutral aluminum dihydride compounds stabilized by tridentate-substituted pyrrolyl ligands: Synthesis, structural characterization and ring-opening polymerization of ε-caprolactone

Chang, Jr-Chiuan,Chen, Ya-Chi,Datta, Amitabha,Lin, Chia-Her,Hsiao, Ching-Sheng,Huang, Jui-Hsien

, p. 3673 - 3680 (2011)

A series of aluminum compounds containing tridentate pyrrolyl ligands were obtained from related aluminum dihydride compounds via protonolysis. Treatment of tetranuclear aluminum compound [C4H2N{2,5-(CH 2NMe2)2}Al2H5] 2 (1) with two equivalents of [C4H3N{2,5- (CH2NMe2)2}] in methylene chloride at 0 °C led to the formation of [C4H2N{2,5-(CH2NMe 2)2}]AlH2 (2). Similarly, when the deuterated aluminum compound 1D was used, the corresponding aluminum compound [C 4H2N{2,5-(CH2NMe2) 2}]AlD2 (2D) could be isolated. The reaction of 2 with one or two equivalents of phenylethyne, triphenylmethanethiol, 2,6- diisopropylaniline, or triphenylsilanol generated mononuclear aluminum compounds [[C4H2N{2,5-(CH2NMe2) 2}]AlRR′ (3, R = -CCPh, R′ = H; 4, R = R′ = -CCPh; 5, R = -SCPh3, R′ = H; 6, R = R′ = -SCPh3; 7, R = -NH(2,6-iPr2Ph), R′ = H; 8, R = R′ = -NH(2,6-iPr2Ph); 9, R = -OSiPh3, R′ = H; 10, R = R′ = -OSiPh3). Related Al-D compounds of 3, 5, 7 and 9 were also synthesized and corresponding IR spectroscopic data well matched in comparison of the stretching frequencies of Al-H and Al-D. The molecular structures of 2D, 4, 5, 5D, 7, and 10 have been determined by X-ray crystallography. Compounds 2, 5, and 7 initiated the ring-opening polymerization of ε-caprolactone and produced high-molecular weight of poly-ε-caprolactone.

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