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Detail of "39637-74-6"

  • CAS Number:
  • 39637-74-6
  • Name:

  • (-)-Camphanoyl chloride

  • Molecular Structure:
  • Formula:
  • C10H13ClO3
  • Molecular Weight:
  • 216.66
  • Synonyms:
  • 2-Oxabicyclo[2.2.1]heptane-1-carbonylchloride, 4,7,7-trimethyl-3-oxo-, (1S)-;(-)-(1S)-Camphanoyl chloride;(-)-(1S,4R)-Camphanoyl chloride;(-)-(S)-Camphanyl chloride;(-)-Camphanic acidchloride;(-)-Camphanic chloride;(-)-Camphanylchloride;(1S)-(-)-Camphanic acid chloride;(1S)-(-)-Camphanic chloride;(1S)-(-)-Camphanoyl chloride;(1S)-(-)-Camphanylchloride;(1S)-(-)-w-Camphanic chloride;(1S)-Camphanoyl chloride;(1S,4R)-(-)-Camphanic acidchloride;(1S,4R)-w-Camphanoyl chloride;(S)-Camphanic acid chloride;(S)-Camphanoylchloride;
  • EINECS:
  • 254-552-4
  • Density:
  • 1.298 g/cm3
  • Melting Point:
  • 71-73 °C(lit.)
  • Boiling Point:
  • 299.5 °C at 760 mmHg
  • Flash Point:
  • 125 °C
  • Solubility:
  • decomposes in water
  • Appearance:
  • Off-white powder
  • Hazard Symbols:
  • CorrosiveC, IrritantXi
  • Risk Codes:
  • 34-29
  • Safety:
  • 26-36/37/39-45-8-27 Details
  • Transport Information:
  • UN 3261 8/PG 2
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CAS No.39637-74-6 (-)-Camphanoyl chlorideCompetitive Product

go to www.baochengchem.com,you can know more about it.

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CAS No.39637-74-6 (-)-Camphanoyl chloride

Assay:98%

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CAS No.39637-74-6 (-)-Camphanoyl chloride

(-)-(1S,4R)-Camphanoyl chloride

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CAS No.39637-74-6 (-)-Camphanoyl chloride

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CAS No.39637-74-6 (-)-Camphanoyl chloride

(-)-Camphanic Chloride

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CAS No.39637-74-6 (-)-Camphanoyl chloride

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CAS No.39637-74-6 (-)-Camphanoyl chloride

Chemical Name: (-)-CAMPHANIC ACID CHLORIDE CAS No. 39637-74-6 Molecular Formula: C10H13ClO3 Formula Weight: 216.66 Property mp : 71-73 °C(lit.) storage temp. : ?20°C Safety Hazard Codes : C Risk Statements : 34 Safety Statements : 26-36/37/39-45 RIDADR : UN 32

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CAS No.39637-74-6 (-)-Camphanoyl chloride

M.W: 216.72 Appearance: white crystalline powder Usage: pharamceutical intermediate Package: 25kg in cardboard drum Quality index: Content: ≥98.0% M.P.: 67-70°c [α]D20(C=1.01 dioxane): -17.9°

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CAS No.39637-74-6 (-)-Camphanoyl chloride

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CAS No.39637-74-6 (-)-Camphanoyl chloride

(1S)-(-)-CAMPHANIC ACID CHLORIDE

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CAS No.39637-74-6 (-)-Camphanoyl chloride

(-)-CAMPHANIC ACID CHLORIDE

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Reference

Enantiodifferentiation of odor perception of a-ambrinols
Enantiodifferentiation of odor perception of a-ambrinols.. Naegeli, P.; Wirz-Habersack, Y. (Givaudan-Roure, Duebendorf 8600, Switz.).Several reagents with their cas registry numbers 39637-74-6 and 65759-55-9 are used here. Tetrahedron: Asymmetry, 3(2), 221-2 (English) 1992. CODEN: TASYE3. ISSN: 0957-4166. DOCUMENT TYPE: Journal CA Section: 30 (Terpenes and Terpenoids) Section cross-reference(s): 62 Racemic a-ambrinol (I) was resolved by fractional crystn. of the diastereomeric mixt. of its (-)-(1S)-camphanic acid esters and subsequent redn. of the CP diastereoisomers with lithium aluminum hydride. .
General Scope of 1,4-Diastereoselective Additions to a 2(3H)-Quinazolinone: Practical Preparation of HIV Therapeutics
General Scope of 1,4-Diastereoselective Additions to a 2(3H)-Quinazolinone: Practical Preparation of HIV Therapeutics. Magnus, Nicholas A.; Confalone, Pat N.; Storace, Louis; Patel, Mona; Wood, Christopher C.; Davis, Wayne P.; Parsons, Rodney L.There are some reagents like 39637-74-6 is used in this study., Jr. ( Chemical Process Research and Development Department, Pharmaceutical Research Institute, Bristol-Myers Squibb Company, Deepwater, NJ 08023-0999, USA). Journal of Organic Chemistry, 68(3), 754-761 (English) 2003 American Chemical Society. CODEN: JOCEAH. ISSN: 0022-3263. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) The practical and highly diastereoselective syntheses of CF3-substituted dihydroquinazolinones via 1,4-addns. of nucleophiles to 2(3H)-quinazolinone I, bearing a chiral auxiliary, was developed. This methodol. 39637-74-6 is the cas registry number of certain chemical which is used as reagents here. was applied to the syntheses of the NNRTIs (nonnucleoside reverse transcriptase inhibitors) II [R = cyclopropylethynyl, (E)-2-cyclopropylvinyl], which are useful for the treatment of HIV (human immunodeficiency virus). The synthesis of II (R = cyclopropylethynyl) required three steps, proceeded in >55% overall yield from the keto aniline III, and gave synthetic access to II [R = (E)-2-cyclopropylvinyl]. ..
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