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3-benzyl-1,5-diphenyl-1H-pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74441-34-2

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74441-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74441-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,4 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74441-34:
(7*7)+(6*4)+(5*4)+(4*4)+(3*1)+(2*3)+(1*4)=122
122 % 10 = 2
So 74441-34-2 is a valid CAS Registry Number.

74441-34-2Downstream Products

74441-34-2Relevant academic research and scientific papers

Visible-light promoted one-pot synthesis of pyrazoles from alkynes and hydrazines

Meng, Yunge,Zhang, Te,Gong, Xinchi,Zhang, Min,Zhu, Chunyin

supporting information, p. 171 - 174 (2018/12/11)

A visible-light promoted cascade of Glaser coupling/annulation has been developed for one-pot synthesis of polysubstituted pyrazoles from alkynes and hydrazines. The method features mild reaction conditions, readily availible starting materials and green

Method for preparing polysubstituted pyrazole through one-pot reaction of substituted alkyne and hydrazine or hydrazine substitute

-

Paragraph 0016; 0017; 0026; 0027, (2019/02/04)

The invention belongs to the technical field of drug intermediate preparation and specifically relates to a method for preparing polysubstituted pyrazole through one-pot reaction of substituted alkyneand hydrazine or hydrazine substitute. The polysubstitu

Access to 2,5-diamidopyrroles and 2,5-diamidofurans by Au(I)-catalyzed double hydroamination or hydration of 1,3-diynes

Kramer, Soren,Madsen, Julie L. H.,Rottlaender, Mario,Skrydstrup, Troels

supporting information; experimental part, p. 2758 - 2761 (2010/08/22)

(Figure presented) A Au(I)-catalyzed hydroamination or hydration of 1,3-diynes to access 2,5-diamidopyrroles and 2,5-diamidofurans has been developed. This method can also be expanded to 2,5-disubstituted furans and 1,2,5-trisubstituted pyrroles including the formation of deuterated heterocycles and 18O-labeled furans.

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