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1,4-bis(2-(thiobenzoylthio)prop-2-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 201611-82-7 Structure
  • Basic information

    1. Product Name: 1,4-bis(2-(thiobenzoylthio)prop-2-yl)benzene
    2. Synonyms: 1,4-bis(2-(thiobenzoylthio)prop-2-yl)benzene
    3. CAS NO:201611-82-7
    4. Molecular Formula:
    5. Molecular Weight: 466.756
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 201611-82-7.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: 1,4-bis(2-(thiobenzoylthio)prop-2-yl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-bis(2-(thiobenzoylthio)prop-2-yl)benzene(201611-82-7)
    11. EPA Substance Registry System: 1,4-bis(2-(thiobenzoylthio)prop-2-yl)benzene(201611-82-7)
  • 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: 201611-82-7(Hazardous Substances Data)

201611-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201611-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,6,1 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 201611-82:
(8*2)+(7*0)+(6*1)+(5*6)+(4*1)+(3*1)+(2*8)+(1*2)=77
77 % 10 = 7
So 201611-82-7 is a valid CAS Registry Number.

201611-82-7Downstream Products

201611-82-7Relevant articles and documents

A facile synthesis route to thiol-functionalized α,ω-telechelic polymers via reversible addition fragmentation chain transfer polymerization

Patton, Derek L.,Mullings, Matthew,Fulghum, Timothy,Advincula, Rigoberto C.

, p. 8597 - 8602 (2005)

A straightforward procedure to α,ω-thiol telechelics was analyzed on the basis of reversible addition fragmentation chain transfer (RAFT) polymerization. It was observed that this technique allows α,ω- thiol functionalized polymers to be prepared directly

A drug-delivery vehicle combining the targeting and thermal ablation of HER2+ breast-cancer cells with triggered drug release

You, Jin-Oh,Guo, Peng,Auguste, Debra T.

, p. 4141 - 4146 (2013)

Covering all three bases: Drug-delivery vehicles that encapsulate doxorubicin (Dox) within a pH-sensitive matrix embedded with gold nanoparticles were synthesized with Herceptin-poly(ethylene glycol) conjugates on the surface for the specific binding of c

End-linked poly[2-(dimethylamino)ethyl methacrylate]-poly(methacrylic acid) polyampholyte conetworks: Synthesis by sequential RAFT polymerization and swelling and SANS characterization

Pafiti, Kyriaki S.,Philippou, Zelina,Loizou, Elena,Porcar, Lionel,Patrickios, Costas S.

body text, p. 5352 - 5362 (2012/04/17)

Four well-defined end-linked triblock polyampholyte conetworks composed of positively ionizable 2-(dimethylamino)ethyl methacrylate (DMAEMA) repeating units and negatively ionizable methacrylic acid (MAA) repeating units were synthesized using one-pot, sequential reversible addition-fragmentation chain transfer (RAFT) polymerization, by employing 1,4-bis[2-(thiobenzoylthio)prop-2- yl]benzene (1,4-BTBTPB) as the chain transfer agent, and ethylene glycol dimethacrylate (EGDMA) as the cross-linker. From the four end-linked conetworks, three were based on ABA triblock polyampholytes with polyDMAEMA midblocks with a constant degree of polymerization (DP) and polyMAA end-blocks of different DPs. The fourth end-linked polyampholytic conetwork was based on an equimolar BAB triblock polyampholyte with a polyMAA midblock. Furthermore, two polyampholyte networks were also prepared: one based on an end-linked equimolar statistical polyampholyte, and one with a randomly cross-linked, rather than an end-linked, architecture. Finally, the two homopolymer networks based on the DMAEMA and the MAA monomers were also synthesized. The MAA units were introduced in the (co)networks via the polymerization of 2-tetrahydropyranyl methacrylate (THPMA) followed by its acid hydrolysis after (co)network formation. The linear precursors to the (co)networks were found to have molecular weights and compositions close to the expected values, whereas the extractables from the (co)networks were determined to be lower than 30%. In water, the degrees of swelling (DS) of all the polyampholyte (co)networks presented a characteristic minimum at intermediate pH values, around the (co)network isoelectric point (pI), while they increased at acidic and basic pHs. The pI values of the ampholytic (co)networks were estimated as the midpoints of the regions of reduced swelling and ranged between 5.3 and 6.8, decreasing with the increase of the MAA content in the (co)networks. Finally, small-angle neutron scattering (SANS) studies of the polyampholyte (co)networks swollen in D2O provided SANS profiles without any peaks but broad shoulders whose location was consistent with the spacing of the cross-linking cores.

POLYMERIZATION WITH LIVING CHARACTERISTICS

-

, (2008/06/13)

This invention concerns a free radical polymerization process, selected chain transfer agents employed in the process and polymers made thereby, in which the process comprises preparing polymer of general Formula (A) and Formula (B) comprising contacting: (i) a monomer selected from the group consisting of vinyl monomers (of structure CH2═CUV), maleic anhydride, N-alkylmaleimide, N-arylmaleimide, dialkyl fumarate and cyclopolymerizable monomers; (ii) a thiocarbonylthio compound selected from Formula (C) and Formula (D) having a chain transfer constant greater than about 0.1; and (iii) free radicals produced from a free radical source; the polymer of Formula (A) being made by contacting (i), (ii) C and (iii) and that of Formula (B) by contacting (i), (ii) D, and (iii); and (iv) controlling the polydispersity of the polymer being formed by varying the ratio of the number of molecules of (ii) to the number of molecules of (iii); wherein Q, R, U, V, Z, Z′, m, p and q are as defined in the text.

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