Cas 76763-85-4,Benzoic acid (1R,2R,6S,7S)-4,4-dimethyl-10-oxo-3,5,9,12-tetraoxa-tricyclo[5.4.1.0<sup>2,6</sup>]dodec-2-ylmethyl ester

76763-85-4

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Basic information

Product Name: Benzoic acid (1R,2R,6S,7S)-4,4-dimethyl-10-oxo-3,5,9,12-tetraoxa-tricyclo[5.4.1.0^2,6]dodec-2-ylmethyl ester
Synonyms:
CAS NO:76763-85-4
Molecular Formula:
Molecular Weight: 348.353
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: Benzoic acid (1R,2R,6S,7S)-4,4-dimethyl-10-oxo-3,5,9,12-tetraoxa-tricyclo[5.4.1.0^2,6]dodec-2-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (1R,2R,6S,7S)-4,4-dimethyl-10-oxo-3,5,9,12-tetraoxa-tricyclo[5.4.1.0^2,6]dodec-2-ylmethyl ester(76763-85-4)
EPA Substance Registry System: Benzoic acid (1R,2R,6S,7S)-4,4-dimethyl-10-oxo-3,5,9,12-tetraoxa-tricyclo[5.4.1.0^2,6]dodec-2-ylmethyl ester(76763-85-4)

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: 76763-85-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76763-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,6 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76763-85:
(7*7)+(6*6)+(5*7)+(4*6)+(3*3)+(2*8)+(1*5)=174
174 % 10 = 4
So 76763-85-4 is a valid CAS Registry Number.

76763-85-4Upstream product

76763-75-2 Benzoic acid (1R,2R,6S,7S)-4,4-dimethyl-9-oxo-3,5,11-trioxa-tricyclo[5.3.1.0^2,6]undec-2-ylmethyl ester

76763-85-4Downstream Products

76763-85-4Relevant academic research and scientific papers

REMOTE SUBSTITUENT EFFECTS IN THE BAEYER-VILLIGER OXIDATION. II. REGIOSELECTION BASED ON THE HYDROXYL GROUP ORIENTATION IN THE TETRAHEDRAL INTERMEDIATE

Noyori, R.,Kobayashi, H.,Sato, T.

, p. 2573 - 2576 (1980)

A remote directing effect in the Baeyer-Villiger oxidation of 8-oxabicyclo-octan-3-one derivatives has been interpreted in terms of chiral orientation of the hydroxyl nonbonding electron pairs in the tetrahedral intermediates.

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