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CAS

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29671-64-5

1,2-bis(1,3-diphenylpropan-2-yl)disulfane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29671-64-5 Structure

  • Basic information

    1. Product Name: 1,2-bis(1,3-diphenylpropan-2-yl)disulfane
    2. Synonyms: 1,2-bis(1,3-diphenylpropan-2-yl)disulfane
    3. CAS NO:29671-64-5
    4. Molecular Formula:
    5. Molecular Weight: 454.7
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29671-64-5.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: 1,2-bis(1,3-diphenylpropan-2-yl)disulfane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-bis(1,3-diphenylpropan-2-yl)disulfane(29671-64-5)
    11. EPA Substance Registry System: 1,2-bis(1,3-diphenylpropan-2-yl)disulfane(29671-64-5)

  • 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: 29671-64-5(Hazardous Substances Data)

29671-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29671-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,7 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29671-64:
(7*2)+(6*9)+(5*6)+(4*7)+(3*1)+(2*6)+(1*4)=145
145 % 10 = 5
So 29671-64-5 is a valid CAS Registry Number.

29671-64-5Relevant articles and documents

Synthesis of 3,3,5,5-tetrabenzyl-1,2,4-trithiol and 1,2-dis(1,3-arylpropan- 2-yl)disulfane

Feng, Fu,Huang, Meng,Duan, Zheng-Chao,Hu, Wei-Bing

, p. 909 - 911 (2013/09/24)

Novel sulfur-containing compounds (3a-3c, 4a-4c) were obtained in ethanol with 1,3-diphenyl-2-propanone as the starting material. The advantages of this procedure were mild reaction conditions, simple protocol, and high yields. The structures of the products were characterized by IR, 1H NMR, MS and elementary analysis. The crystal of the new compound 4a belongs to monoclinic, space group C2 with a = 18.727(3), b = 6.5179(9), c = 13.7576(18) ?, β = 131.0610(10), V = 1266.2(3)?3, Z = 2, Dc = 2.136 g/cm3, μ = 1.078 mm-1, F(0 0 0) = 843, R = 0.0490 and wR = 0.1247 for 3211 observed reflection with I > 2σ(I). X-ray analysis reveals that the molecule is not symmetrical, the molecular structure is stabilized by weak π-π stacking interactions, and no classical hydrogen bonds can be observed.

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