Cas 482636-03-3,(2S,3S,4R,5S)-[5-benzyloxy-3,4-(cyclohexylidenedioxy)tetrahydropyran-2-yl]-acetic acid

482636-03-3

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Basic information

Product Name: (2S,3S,4R,5S)-[5-benzyloxy-3,4-(cyclohexylidenedioxy)tetrahydropyran-2-yl]-acetic acid
Synonyms: (2S,3S,4R,5S)-[5-benzyloxy-3,4-(cyclohexylidenedioxy)tetrahydropyran-2-yl]-acetic acid
CAS NO:482636-03-3
Molecular Formula:
Molecular Weight: 362.423
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2S,3S,4R,5S)-[5-benzyloxy-3,4-(cyclohexylidenedioxy)tetrahydropyran-2-yl]-acetic acid(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,4R,5S)-[5-benzyloxy-3,4-(cyclohexylidenedioxy)tetrahydropyran-2-yl]-acetic acid(482636-03-3)
EPA Substance Registry System: (2S,3S,4R,5S)-[5-benzyloxy-3,4-(cyclohexylidenedioxy)tetrahydropyran-2-yl]-acetic acid(482636-03-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 482636-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 482636-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,2,6,3 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 482636-03:
(8*4)+(7*8)+(6*2)+(5*6)+(4*3)+(3*6)+(2*0)+(1*3)=163
163 % 10 = 3
So 482636-03-3 is a valid CAS Registry Number.

482636-03-3Upstream product

482636-03-3Downstream Products

482636-03-3Relevant academic research and scientific papers

Enantioselective Deprotonation of meso-Cycloheptanone Derivative: Application to the Synthesis of a Potential Intermediate for Pseudomonic Acid B

Honda, Toshio,Kimura, Nobuaki

, p. 4567 - 4570 (2007/10/03)

(Matrix Presented) A novel synthetic path to a potential intermediate for the synthesis of pseudomonic acid B was established by employing enantioselective deprotonation of a meso-cycloheptanone derivative bearing hydroxy groups at the 3,4,5,6-positions w

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