607357-44-8 Usage
Explanation
1,3-Cyclopentanedicarboxamide,(1R,3R)-rel-(9CI) is derived from cyclopentane, a five-membered ring of carbon atoms. The presence of this ring structure is a key feature of the compound.
3. Amide Functional Group
Explanation
The compound contains an amide functional group, which is a carbonyl (C=O) group bonded to a nitrogen atom with a single bond. This group is important for the compound's reactivity and potential applications.
Explanation
The compound has a specific arrangement of atoms at the chiral centers, denoted by the (1R,3R)-rel configuration. This refers to the spatial arrangement of the atoms around the chiral centers, which can affect the compound's properties and reactivity.
Explanation
Although not widely documented, the presence of the amide functional group suggests that 1,3-Cyclopentanedicarboxamide,(1R,3R)-rel-(9CI) may be useful in the synthesis of other organic compounds or in pharmaceutical research. Further studies are needed to confirm these potential applications.
7. Need for Further Research
Explanation
The exact properties and uses of 1,3-Cyclopentanedicarboxamide, (1R,3R)-rel-(9CI) are not well understood, and more research is needed to fully explore its potential applications and properties.
Chiral Centers
2
5. (1R,3R)-rel Configuration
Potential Applications
Synthesis of other organic compounds, pharmaceutical research
Check Digit Verification of cas no
The CAS Registry Mumber 607357-44-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,7,3,5 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 607357-44:
(8*6)+(7*0)+(6*7)+(5*3)+(4*5)+(3*7)+(2*4)+(1*4)=158
158 % 10 = 8
So 607357-44-8 is a valid CAS Registry Number.
607357-44-8Relevant articles and documents
Corresponding amine nitrile and method of manufacturing thereof
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Paragraph 0124; 0125; 0129, (2018/07/15)
The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.
Corresponding amine nitrile and method of manufacturing thereof
-
Paragraph 0125; 0129, (2017/10/22)
The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.
Corresponding amine nitrile and method of manufacturing thereof
-
Paragraph 0123; 0124; 0127; 0128, (2017/10/22)
The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.
