CAS 39637-74-6

(-)-Camphanoyl chloride

Description:

(-)-Camphanoyl chloride, with the CAS number 39637-74-6, is an organic compound derived from camphor. It is characterized by its acyl chloride functional group, which makes it a reactive intermediate in organic synthesis. This compound typically appears as a colorless to pale yellow liquid with a pungent odor. (-)-Camphanoyl chloride is known for its ability to undergo acylation reactions, making it useful in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. It is soluble in organic solvents such as dichloromethane and ether but is generally insoluble in water due to its hydrophobic nature. The compound should be handled with care, as it can be corrosive and irritating to the skin, eyes, and respiratory system. Proper safety precautions, including the use of personal protective equipment, are essential when working with this substance in a laboratory setting. Overall, (-)-Camphanoyl chloride serves as a valuable reagent in synthetic organic chemistry.

Formula: C₁₀H₁₃ClO₃

InChI: InChI=1S/C10H13ClO3/c1-8(2)9(3)4-5-10(8,6(11)12)14-7(9)13/h4-5H2,1-3H3/t9-,10+/m0/s1

InChI key: InChIKey=PAXWODJTHKJQDZ-VHSXEESVSA-N

SMILES: C(Cl)(=O)[C@]12C(C)(C)[C@](C)(C(=O)O1)CC2

Synonyms:

• (-)-(1S)-Camphanoyl chloride
• (-)-(S)-Camphanyl chloride
• (-)-Camphanic acid chloride
• (-)-Camphanic chloride
• (-)-Camphanoyl chloride
• (-)-Camphanyl chloride
• (1S)-(-)-Camphanic Acid Chloride
• (1S)-(-)-Camphanic chloride
• (1S)-(-)-Camphanyl chloride
• (1S)-(-)-ω-Camphanic chloride
• (1S,4R)-(-)-Camphanic acid chloride
• (1S,4R)-4,7,7-trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carbonyl chloride
• (1S,4R)-ω-Camphanoyl chloride
• (S)-Camphanic acid chloride
• (S)-Camphanoyl chloride
• 2-Oxabicyclo[2.2.1]heptane-1-carbonyl chloride, 4,7,7-trimethyl-3-oxo-, (1S)-
• 2-Oxabicyclo[2.2.1]heptane-1-carbonyl chloride, 4,7,7-trimethyl-3-oxo-, (1S,4R)-

(-)-Camphanic Chloride

CAS: 39637-74-6

Formula: C₁₀H₁₃ClO₃

Purity: >97.0%(T)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 216.66

Ref: 3B-C1022

(1S)-(-)-Camphanic chloride, 95%

CAS: 39637-74-6

(1S)-(-)-Camphanic chloride is used as a resolving agent for alcohols as the diastereomeric esters by crystallization or chromatography and as a chiral derivatization reagent for determination of enantiomeric excess of alcohols and amines. This Thermo Scientific Chemicals brand product was originall

Formula: C₁₀H₁₃ClO₃

Purity: 95%

Color and Shape: White to cream to grey, Powder or crystals of flakes

Molecular weight: 216.66

Ref: 02-L14148

(1S,4R)-4,7,7-Trimethyl-3-oxo-2-oxabicyclo[2.2.1]heptane-1-carbonyl chloride

CAS: 39637-74-6

Formula: C₁₀H₁₃ClO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 216.6614

Ref: IN-DA0032BM

(-)-Camphanic acid chloride

CAS: 39637-74-6

Formula: C₁₀H₁₃ClO₃

Purity: ≥ 98.0%

Color and Shape: White to off-white crystalline powder

Molecular weight: 216.67

Ref: 7W-GK2495

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

CAS: 39637-74-6

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

Formula: C₁₀H₁₃ClO₃

Purity: 98%

Color and Shape: off white crystalline solid

Molecular weight: 216.66g/mol

Ref: 54-OR6501T

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

CAS: 39637-74-6

Formula: C₁₀H₁₃ClO₃

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 216.66

Ref: 10-F471541

Propoxur

Controlled Product

CAS: 39637-74-6

Applications An optically active resolving agent.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Helv. Chim. Acta, 61, 2773 (1978)

Formula: C₁₀H₁₃ClO₃

Color and Shape: Neat

Molecular weight: 216.66

Ref: TR-C165000

(1S)-(-)-Camphanoyl chloride

CAS: 39637-74-6

Camphanoyl chloride is a chemical compound that is derived from camphor. It has inhibitory properties and inhibits the activity of c1-6 alkyl, fatty acids, and nitrogen atoms. Camphanoyl chloride can be used in the liquid chromatograph to separate stereoisomers. This substance is also used as an intermediate in organic syntheses. Camphanoyl chloride can be made by reacting hydrochloric acid with an acyl chain or dialkylamino group. The reaction yield is dependent on the stereochemical orientation of the starting material.

Formula: C₁₀H₁₃ClO₃

Purity: Min. 95%

Color and Shape: White To Tan To Grey Solid

Molecular weight: 216.66 g/mol

Ref: 3D-FC19643