10540-35-9 Usage
General Description
3-Bromo-4'-fluorobiphenyl is a chemical compound with the molecular formula C12H8BrF. It is a derivative of biphenyl, a compound made up of two benzene rings connected by a single bond. This particular derivative has a bromine atom and a fluorine atom attached to the biphenyl structure, resulting in its distinct chemical properties. 3-Bromo-4'-fluorobiphenyl is used in organic synthesis, pharmaceutical research, and as a chemical intermediate in the production of various compounds. Its unique structure and reactivity make it an important building block in the development of new materials and pharmaceuticals. However, it is important to handle this compound with caution, as it can be harmful if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 10540-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,4 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10540-35:
(7*1)+(6*0)+(5*5)+(4*4)+(3*0)+(2*3)+(1*5)=59
59 % 10 = 9
So 10540-35-9 is a valid CAS Registry Number.
10540-35-9Relevant articles and documents
Visible-Light-Promoted, Catalyst-Free Gomberg-Bachmann Reaction: Synthesis of Biaryls
Lee, Juyoung,Hong, Boseok,Lee, Anna
, p. 9297 - 9306 (2019/08/12)
Biaryls were synthesized via a novel visible-light-promoted Gomberg-Bachmann reaction that does not require a photosensitizer or any metal reagents. The formation of an electron donor-acceptor complex between aryl diazonium salts and pyridine allows, under visible-light irradiation, the synthesis of biaryls in moderate-to-high yields.
Insecticidal substituted-2,4-diaminoquinazolines
-
, (2008/06/13)
An insecticidal composition comprising, in admixture with an agriculturally acceptable carrier, an insecticidally effective amount of a 2,4-diaminoquinazoline compound of the formula: STR1 wherein R1, R2, R6, R7, W, X, Y, and Z are as defined herein; methods of using the same; novel 2,4-diaminoquinazolines per se; and intermediates in the preparation thereof.
