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2,4-Diazabicyclo[3.1.0]hexan-3-one,1,5-dimethyl-(9CI) is a cyclic diamine derivative with a molecular formula of C8H14N2O. It is a chemical compound known for its unique ring structure, which provides stability and reactivity for various chemical reactions. This versatile and important chemical in the field of organic chemistry is commonly used as a catalyst in organic synthesis.

174840-87-0

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174840-87-0 Usage

Uses

Used in Pharmaceutical Industry:
2,4-Diazabicyclo[3.1.0]hexan-3-one,1,5-dimethyl-(9CI) is used as a catalyst in the production of pharmaceuticals for its ability to facilitate complex organic transformations, enabling the synthesis of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 2,4-Diazabicyclo[3.1.0]hexan-3-one,1,5-dimethyl-(9CI) is utilized as a catalyst for the synthesis of agrochemicals, contributing to the development of effective and efficient crop protection products.
Used in Specialty Chemicals Production:
2,4-Diazabicyclo[3.1.0]hexan-3-one,1,5-dimethyl-(9CI) is employed as a catalyst in the production of specialty chemicals, where its unique ring structure and reactivity are leveraged to achieve specific chemical transformations required for the synthesis of high-value products.

Check Digit Verification of cas no

The CAS Registry Mumber 174840-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,8,4 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 174840-87:
(8*1)+(7*7)+(6*4)+(5*8)+(4*4)+(3*0)+(2*8)+(1*7)=160
160 % 10 = 0
So 174840-87-0 is a valid CAS Registry Number.

174840-87-0Downstream Products

174840-87-0Relevant academic research and scientific papers

Synthesis of cis-1,5-dimethyl-2,4-dinitro-2,4-diazabicyclo[3.1.0]hexan-3-one and cis-1,5-dimethyl-2,4-dinitro-2,4-diazabicyclo[3.2.0]heptan-3-one

Gagnon, Janet L.,Zajac Jr., Walter W.

, p. 837 - 845 (1996)

cis-1,5-Dimethyl-2,4-dinitro-2,4-diazabicyclo[3.2.0]heptan-3-one and cis-1,5-dimethyl-2,4-dinitro-2,4-diazabicyclo[3.1.0]hexan-3-one were both synthesized in three steps each from a common precursor, 1,3-diacetyl-4,5-dimethyl-4-imidazolin-2-one.

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