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endo-Norborneol

endo-Norborneol is an alcohol.

endo-Norborneol[1]
Names
Preferred IUPAC name
rel-(1R,2S,4S)-Bicyclo[2.2.1]heptan-2-ol
Other names
endo-2-Norborneol; endo-Norbornyl alcohol
Identifiers
  • 61277-90-5 (2R) Y
  • 36779-79-0 (2S) N
3D model (JSmol)
  • (2R): Interactive image
  • (2S): Interactive image
ChemSpider
  • 9030707 (2R)
  • 9150646 (2S) Y
ECHA InfoCard 100.127.627
  • 10855416 (2R)
  • 10975445 (2S)
  • InChI=1/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7-/s2
    Key: ZQTYQMYDIHMKQB-HNBBVXEKNA-N
  • (2R): InChI=1S/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7-/m1/s1
    Key: ZQTYQMYDIHMKQB-DSYKOEDSSA-N
  • (2S): InChI=1S/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7-/m0/s1
    Key: ZQTYQMYDIHMKQB-XVMARJQXSA-N
  • (2R): O[C@@H]1C[C@H]2CC[C@@H]1C2
  • (2S): O[C@H]1C[C@@H]2CC[C@H]1C2
Properties
C7H12O
Molar mass 112.17 g/mol
Melting point 149 to 154 °C (300 to 309 °F; 422 to 427 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)

See also edit

References edit

  1. ^ (+)-endo-2-Norborneol at Sigma-Aldrich

External links edit

  • endo-Norborneol MSDS
  • Reaction of organic compounds under high temperature – dilute acid (HTDA) conditions. III. The perdeuteration of bicyclo[2.2.1]heptanes
  • J. K. Stille, and Fred M. Sonnenberg (1966). "The Reaction of endo- and exo-2-Norborneol with Thionyl Chloride". J. Am. Chem. Soc. 88 (21): 4915–4921. doi:10.1021/ja00973a027.


endo, norborneol, alcohol, names, preferred, iupac, name, bicyclo, heptan, other, names, endo, norborneol, endo, norbornyl, alcohol, identifiers, number, 61277, y36779, model, jsmol, interactive, image, interactive, image, chemspider, 9030707, 9150646, echa, i. endo Norborneol is an alcohol endo Norborneol 1 Names Preferred IUPAC name rel 1R 2S 4S Bicyclo 2 2 1 heptan 2 ol Other names endo 2 Norborneol endo Norbornyl alcohol Identifiers CAS Number 61277 90 5 2R Y36779 79 0 2S N 3D model JSmol 2R Interactive image 2S Interactive image ChemSpider 9030707 2R 9150646 2S Y ECHA InfoCard 100 127 627 PubChem CID 10855416 2R 10975445 2S InChI InChI 1 C7H12O c8 7 4 5 1 2 6 7 3 5 h5 8H 1 4H2 t5 6 7 s2Key ZQTYQMYDIHMKQB HNBBVXEKNA N 2R InChI 1S C7H12O c8 7 4 5 1 2 6 7 3 5 h5 8H 1 4H2 t5 6 7 m1 s1Key ZQTYQMYDIHMKQB DSYKOEDSSA N 2S InChI 1S C7H12O c8 7 4 5 1 2 6 7 3 5 h5 8H 1 4H2 t5 6 7 m0 s1Key ZQTYQMYDIHMKQB XVMARJQXSA N SMILES 2R O C H 1C C H 2CC C H 1C2 2S O C H 1C C H 2CC C H 1C2 Properties Chemical formula C7H12O Molar mass 112 17 g mol Melting point 149 to 154 C 300 to 309 F 422 to 427 K Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox referencesSee also editExo NorborneolReferences edit endo 2 Norborneol at Sigma AldrichExternal links editendo Norborneol MSDS Reaction of organic compounds under high temperature dilute acid HTDA conditions III The perdeuteration of bicyclo 2 2 1 heptanes PDF J K Stille and Fred M Sonnenberg 1966 The Reaction of endo and exo 2 Norborneol with Thionyl Chloride J Am Chem Soc 88 21 4915 4921 doi 10 1021 ja00973a027 nbsp This article about an alcohol is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Endo Norborneol amp oldid 1064104350, wikipedia, wiki, book, books, library,

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