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2,4,6-Tris(pentadecafluoroheptyl)-1,3,5-triazine is a heterocyclic fluorinated building block, which is an s-triazine derivative. It is a white solidified mass or fragments.

21674-38-4

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21674-38-4 Usage

Uses

Used in Mass Spectrometry:
2,4,6-Tris(pentadecafluoroheptyl)-1,3,5-triazine is used as a reference standard in mass spectroscopy for m/z ratios between 600-1600.
Used in Chemical Synthesis:
2,4,6-Tris(pentadecafluoroheptyl)-1,3,5-triazine may be used in chemical synthesis for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 21674-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,7 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21674-38:
(7*2)+(6*1)+(5*6)+(4*7)+(3*4)+(2*3)+(1*8)=104
104 % 10 = 4
So 21674-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C24F45N3/c25-4(26,7(31,32)10(37,38)13(43,44)16(49,50)19(55,56)22(61,62)63)1-70-2(5(27,28)8(33,34)11(39,40)14(45,46)17(51,52)20(57,58)23(64,65)66)72-3(71-1)6(29,30)9(35,36)12(41,42)15(47,48)18(53,54)21(59,60)24(67,68)69

21674-38-4 Well-known Company Product Price

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  • TCI America

  • (T0828)  2,4,6-Tris(pentadecafluoroheptyl)-1,3,5-triazine  >98.0%(GC)

  • 21674-38-4

  • 100mg

  • 890.00CNY

  • Detail

  • Alfa Aesar

  • (L16678)  2,4,6-Tris(perfluoroheptyl)-1,3,5-triazine, Mass Spec Std   

  • 21674-38-4

  • 100mg

  • 560.0CNY

  • Detail

  • Alfa Aesar

  • (L16678)  2,4,6-Tris(perfluoroheptyl)-1,3,5-triazine, Mass Spec Std   

  • 21674-38-4

  • 500mg

  • 1945.0CNY

  • Detail

  • Aldrich

  • (358797)  2,4,6-Tris(pentadecafluoroheptyl)-1,3,5-triazine  98%

  • 21674-38-4

  • 358797-100MG

  • 416.52CNY

  • Detail

21674-38-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tris(1,1,2,2,3,3,4,4,5,5,6,6,7,7,7-pentadecafluoroheptyl)-1,3,5-triazine

1.2 Other means of identification

Product number -
Other names 2,3-DIMETHYL-2,3-BUTANEDIAMINE DIHYDROCHLORIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21674-38-4 SDS

21674-38-4Downstream Products

21674-38-4Relevant academic research and scientific papers

REACTIONS OF PERFLUORONITRILES. II. INTERACTIONS WITH PHENYLPHOSPHINE

Paciorek, K. J. L.,Nakahara, J. H.,Kratzer, R. H.

, p. 269 - 288 (1985)

Treatment of perfluoro-n-octanonitrile with phenylphosphine gave tetraphenyltetraphosphine and a spectrum of reduction and interaction products.Fifteen compounds were identified.The imine, (Rf=C7F15) RfCH=NH, and the amine, RfCH2NH2, were the primary reduction products.Secondary phosphorus-free products, some formed following ammonia evolution, were the following: RfCH=NCH2Rf, RfCH2CH(NH2)Rf, RfC(=NH)N=CRf(NH2), RfCH2NHCRf(=NH), (RfCN)3, RfCH=NCRf=NCRf(=NH), RfCH2N=CRfNHCH2Rf, and RfCH2N=CRfNHCRf(=NH).Only three phosphorus-containing materials were definitely identified: RfCH(NH2)P(C6H5)H, RfCHN=CHRf, and RfC(=NH)P(C6H5)CRf(=NH).Depending on reaction conditions, specific phosphorus-containing compounds could be preferentially produced.All the structure assignments are based solely on mass spectral breakdown patterns, since pure compounds were not isolated.

REACTIONS OF PERFLUORONITRILES. I. INTERACTIONS WITH ANILINE

Paciorek, K. J. L.,Nakahara, J. H.,Kratzer, R. H.

, p. 241 - 250 (1985)

Perfluoro-n-octanonitrile was found to react with aniline both in the absence and presence of solvents.A spectrum of products was formed including tris(perfluoro-n-heptyl)-s-triazine, N-phenyl-perfluoro-n-octylamidine, and N'-(perfluoro-n-octylimidoyl)-N-phenyl-perfluoro-n-octylamidine, as well as the diphenyl analogues of the last two compounds.The reaction mechanisms, infrared and mass spectra are discussed.

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