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2,3-Butanediamine, N,N',2,3-tetraphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56506-64-0 Structure
  • Basic information

    1. Product Name: 2,3-Butanediamine, N,N',2,3-tetraphenyl-
    2. Synonyms:
    3. CAS NO:56506-64-0
    4. Molecular Formula: C28H28N2
    5. Molecular Weight: 392.544
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56506-64-0.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: 2,3-Butanediamine, N,N',2,3-tetraphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-Butanediamine, N,N',2,3-tetraphenyl-(56506-64-0)
    11. EPA Substance Registry System: 2,3-Butanediamine, N,N',2,3-tetraphenyl-(56506-64-0)
  • 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: 56506-64-0(Hazardous Substances Data)

56506-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56506-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,0 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56506-64:
(7*5)+(6*6)+(5*5)+(4*0)+(3*6)+(2*6)+(1*4)=130
130 % 10 = 0
So 56506-64-0 is a valid CAS Registry Number.

56506-64-0Downstream Products

56506-64-0Relevant articles and documents

Reductive Coupling of Aromatic Aldehydes and Ketones under Electrochemical Conditions

Li, Qian-Yu,Swaroop, Toreshettahally R.,Wang, Heng Shan,Wang, Zi-Qiang

, (2020)

Reductive coupling of o-substituted carbonyl compounds and m-substituted carbonyl compounds by the direct transfer of electron to carbonyl group respectively gave 1-(4-(1-hydroxy-1-phenylethyl/methyl)phenyl)ethanones/methanones and 2,3-bis(3-substitutedph

Organic reaction in water. Part 1. A convenient method for reduction of imines using zinc powder

Tsukinoki, Takehito,Mitoma, Yoshiharu,Nagashima, Satoko,Kawaji, Takatoshi,Hashimoto, Iwao,Tashiro, Masashi

, p. 8873 - 8876 (2007/10/03)

Reduction of imines was performed with zinc powder in 5% aqNaOH solution without any organic solvents under mild conditions, and the corresponding amines were obtained in good yields.

Reduction of Schiff's Bases and Phenylhydrazones by Zinc Dust

Khan, Naseem H.,Zuberi, Rashid H.,Siddiqui, Amin A.

, p. 363 - 372 (2007/10/02)

Schiff's bases when subjected to the chemical action of zinc dust and chloroform in ethyl alcohol at steam bath temperature for varying times yield 1,2-diaminophenylethanes in crystalline form and in good yield (Table 1).

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