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(1R,2S,5S)-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carbonitrile is a bicyclic chemical compound with the molecular formula C9H13N. It features a nitrogen heteroatom and a carbonitrile functional group, along with a chiral center that gives rise to multiple stereoisomers, with the (1R,2S,5S) configuration being a notable example. (1R,2S,5S)-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carbonitrile is recognized for its unique structure and chemical reactivity, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals. Its potential extends to the development of new drugs and other bioactive compounds, underpinning its significance in medicinal chemistry.

1037559-82-2

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1037559-82-2 Usage

Uses

Used in Pharmaceutical Synthesis:
(1R,2S,5S)-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carbonitrile serves as a key building block in the creation of various pharmaceuticals. Its unique structure and reactivity allow for the development of complex molecules with specific therapeutic properties, contributing to the advancement of new treatments for a range of diseases and conditions.
Used in Agrochemical Development:
In the agrochemical industry, (1R,2S,5S)-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carbonitrile is utilized for the synthesis of bioactive compounds. Its incorporation into these products can lead to the design of more effective pesticides, herbicides, and other agricultural chemicals that are crucial for maintaining crop health and productivity.
Used in Drug Discovery:
(1R,2S,5S)-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carbonitrile's potential applications extend to drug discovery, where it can be employed as a starting point for the design and synthesis of novel drug candidates. Its unique attributes make it a promising candidate for the development of innovative therapeutic agents that address unmet medical needs.
Used in Bioactive Compound Research:
(1R,2S,5S)-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carbonitrile is also used in research aimed at discovering new bioactive compounds. Its versatility in chemical reactions and its capacity to form a variety of stereoisomers make it an ideal candidate for exploring the properties and potential applications of new molecules in biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 1037559-82-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,5,5 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1037559-82:
(9*1)+(8*0)+(7*3)+(6*7)+(5*5)+(4*5)+(3*9)+(2*8)+(1*2)=162
162 % 10 = 2
So 1037559-82-2 is a valid CAS Registry Number.

1037559-82-2Upstream product

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