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(3-Mercaptopropionyl)benzylamine is an organic compound with the chemical formula C10H14N2S. It is a derivative of benzylamine, featuring a 3-mercaptopropionyl group attached to the benzylamine structure. (3-mercaptopropionyl)benzylamine is characterized by the presence of a thiol (-SH) group, which provides it with unique chemical properties, such as the ability to form disulfide bonds with other molecules containing thiol groups. It is used in various chemical reactions and can be found in research and industrial applications, particularly in the synthesis of pharmaceuticals and other specialty chemicals. Due to its reactivity, it is typically handled with care in a controlled environment.

2935-92-4

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2935-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2935-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2935-92:
(6*2)+(5*9)+(4*3)+(3*5)+(2*9)+(1*2)=104
104 % 10 = 4
So 2935-92-4 is a valid CAS Registry Number.

2935-92-4Relevant academic research and scientific papers

All Non-Carbon B3NO2 Exotic Heterocycles: Synthesis, Dynamics, and Catalysis

Opie, Christopher R.,Noda, Hidetoshi,Shibasaki, Masakatsu,Kumagai, Naoya

supporting information, p. 4648 - 4653 (2019/03/17)

The B3NO2 six-membered heterocycle (1,3-dioxa-5-aza-2,4,6-triborinane=DATB), comprising three different non-carbon period 2 elements, has been recently demonstrated to be a powerful catalyst for dehydrative condensation of carboxylic acids and amines. The tedious synthesis of DATB, however, has significantly diminished its utility as a catalyst, and thus the inherent chemical properties of the ring system have remained virtually unexplored. Here, a general and facile synthetic strategy that harnesses a pyrimidine-containing scaffold for the reliable installation of boron atoms is disclosed, giving rise to a series of Pym-DATBs from inexpensive materials in a modular fashion. The identification of a soluble Pym-DATB derivative allowed for the investigation of the dynamic nature of the B3NO2 ring system, revealing differential ring-closing and -opening behaviors depending on the medium. Readily accessible Pym-DATBs proved their utility as efficient catalysts for dehydrative amidation with broad substrate scope and functional-group tolerance, offering a general and practical catalytic alternative to reagent-driven amidation.

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