(1R:2R)-Pinanone-(3)-semicarbazone is a chiral compound derived from pinanone, a bicyclic ketone found in the essential oils of pine trees. This specific semicarbazone derivative is characterized by its 1R,2R configuration, indicating that both the hydroxyl-bearing carbons are in the R configuration. The compound is formed by the reaction of pinanone with semicarbazide, resulting in the formation of a semicarbazone moiety attached to the carbonyl group of pinanone. This derivative is of interest in the field of organic chemistry, particularly in the study of chiral compounds and their applications in synthesis and analysis. It may also have potential applications in the development of new pharmaceuticals or as a chiral auxiliary in asymmetric synthesis.

1741-39-5

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Basic information
1. Product Name: (1R:2R)-pinanone-⁽³⁾-semicarbazone
2. Synonyms:
3. CAS NO:1741-39-5
4. Molecular Formula:
5. Molecular Weight: 209.291
6. EINECS: N/A
7. Product Categories: N/A
Chemical Properties
1. Melting Point: N/A
2. Boiling Point: N/A
3. Flash Point: N/A
4. Appearance: N/A
5. Density: N/A
6. Refractive Index: N/A
7. Storage Temp.: N/A
8. Solubility: N/A
9. CAS DataBase Reference: (1R:2R)-pinanone-⁽³⁾-semicarbazone(CAS DataBase Reference)
10. NIST Chemistry Reference: (1R:2R)-pinanone-⁽³⁾-semicarbazone(1741-39-5)
11. EPA Substance Registry System: (1R:2R)-pinanone-⁽³⁾-semicarbazone(1741-39-5)
Safety Data
1. Hazard Codes: N/A
2. Statements: N/A
3. Safety Statements: N/A
4. WGK Germany:
5. RTECS:
6. HazardClass: N/A
7. PackingGroup: N/A
8. Hazardous Substances Data: 1741-39-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1741-39-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1741-39:
(6*1)+(5*7)+(4*4)+(3*1)+(2*3)+(1*9)=75
75 % 10 = 5
So 1741-39-5 is a valid CAS Registry Number.

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