What is the D-CAMPHOR?

D-CAMPHOR is white crystals, while it's Molecular Formula is C10H16O. white crystals analgesic, antiinfective, antipruritic

What is the CAS number for D-CAMPHOR?

The CAS number of D-CAMPHOR is 464-49-3.

What is D-CAMPHOR (464-49-3) used for?

(1R)-(+)-Camphor is a terpene that has been found in C. sativa, C. indica, and C. sativa/C. indica hybrid strains as well as the essential oils from a variety of herbs including rosemary, lavender, and sage and has diverse biological activities. It inhibits norepinephrine secretion and cytosolic calcium and sodium increases induced by the nicotinic acetylcholine receptor (nAChR) agonist 1,1-dimethyl-4-phenylpiperazinium iodide (DMPP) in chromaffin cells (IC50s = 70, 88, and 19 μM, respectively). (1R)-(+)-Camphor (65-260 μM) induces proliferation of and increases expression of collagen IA, collagen IIIA, collagen IVA, and elastin in human primary dermal fibroblasts. In vivo, (1R)-(+)-camphor increases expression of collagen IA, collagen IIIA, collagen IVA, and elastin in skin in UV-exposed mice when administered at doses of 26 and 55 mM in drinking water post UV-exposure. It reduces cough frequency in citric acid-challenged guinea pigs. (1R)-(+)-Camphor is insecticidal, reducing digging activity and inducing mortality of fire ant workers. It has also been used as a building block in the synthesis of cannabinergic ligands.InChI:InChI=1/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7?,10-/m0/s1

What is the D-CAMPHOR?

D-CAMPHOR is white crystals, while it's Molecular Formula is C10H16O. white crystals analgesic, antiinfective, antipruritic

What is the CAS number for D-CAMPHOR?

The CAS number of D-CAMPHOR is 464-49-3.

What is D-CAMPHOR (464-49-3) used for?

(1R)-(+)-Camphor is a terpene that has been found in C. sativa, C. indica, and C. sativa/C. indica hybrid strains as well as the essential oils from a variety of herbs including rosemary, lavender, and sage and has diverse biological activities. It inhibits norepinephrine secretion and cytosolic calcium and sodium increases induced by the nicotinic acetylcholine receptor (nAChR) agonist 1,1-dimethyl-4-phenylpiperazinium iodide (DMPP) in chromaffin cells (IC50s = 70, 88, and 19 μM, respectively). (1R)-(+)-Camphor (65-260 μM) induces proliferation of and increases expression of collagen IA, collagen IIIA, collagen IVA, and elastin in human primary dermal fibroblasts. In vivo, (1R)-(+)-camphor increases expression of collagen IA, collagen IIIA, collagen IVA, and elastin in skin in UV-exposed mice when administered at doses of 26 and 55 mM in drinking water post UV-exposure. It reduces cough frequency in citric acid-challenged guinea pigs. (1R)-(+)-Camphor is insecticidal, reducing digging activity and inducing mortality of fire ant workers. It has also been used as a building block in the synthesis of cannabinergic ligands.InChI:InChI=1/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7?,10-/m0/s1

D-CAMPHOR

Basic information

Product Name:D-CAMPHOR
CasNo.:464-49-3
MF:C₁₀H₁₆O

Physical and Chemical Properties

Purity:99%
Melting Point:179-181 °C(lit.)
Appearance:white crystals

Inquiry

Product Details

CasNo： 464-49-3

MF： C₁₀H₁₆O

Appearance： white crystals

Export Top Purity D-CAMPHOR 464-49-3 In Stock

Molecular Formula:C10H16O
Molecular Weight:152.236
Appearance/Colour:white crystals
Vapor Pressure:4 mm Hg ( 70 °C)
Melting Point:179-181 °C(lit.)
Refractive Index:44.5 ° (C=20, EtOH)
Boiling Point:207.4 °C at 760 mmHg
Flash Point:64.4 °C
PSA：17.07000
Density:0.982 g/cm³
LogP:2.40170
IDLH:1395
IDLH:140
IDLH:2230

D-CAMPHOR(Cas 464-49-3) Usage

D-Camphor is an organic compound with a special smell and properties. In the field of medicine, it has certain medicinal value, such as stimulating local blood circulation and relieving pain, and is often used in some external medicines. In industry, D-Camphor can be used to make products such as spices and insect repellents. Its volatility and unique smell make it play a role in insect repellent and deodorization. However, it should be noted that D-Camphor has a certain toxicity and should be used in accordance with relevant regulations and safety guidelines. D-Camphor is generally extracted from plants of the Lauraceae family or prepared by chemical synthesis.

InChI:InChI=1/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7?,10-/m0/s1

464-49-3 Relevant articles

Desymmetrization of cyclohexadienones viad-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction

Min-Qiang Jiaa and Shu-Li You*a

, Chemical Communications, Issue 51, 2012

Enantioselective desymmetrization of cyclohexadienones via a D-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction was realized. With 10 mol% of camphor-derived triazolium salt E and 10 mol% of DIEA, various substituted cyclohexadienones proceeded through an intramolecular Stetter reaction, affording tricyclic products in moderate to good yields and excellent ee.

Dysprosium-doped zinc tungstate nanospheres as highly efficient heterogeneous catalysts in green oxidation of terpenic alcohols with hydrogen peroxide

Batalha, Daniel Carreira,Mesquita Borges, Kellen Cristina,de Fátima Gon?alves, Rosana,de Matos Rodrigues, Murillo Henrique,Godinho, Mário Júnior,Fajardo, Humberto Vieira,de Oliveira Bruziquesi, Carlos Giovani,da Silva, Márcio José

, p. 6661 - 6670 (2021/04/22)

A green route to oxidize terpenic alcoho...

A Structural View on the Stereospecificity of Plant Borneol-Type Dehydrogenases

Chánique, Andrea M.,Dimos, Nicole,Drienovská, Ivana,Calderini, Elia,Pantín, Mónica P.,Helmer, Carl P. O.,Hofer, Michael,Sieber, Volker,Parra, Loreto P.,Loll, Bernhard,Kourist, Robert

, p. 2262 - 2277 (2021/03/16)

The development of sustainable processes...

464-49-3 Process route

: 2792-42-9
(R,R)-camphor oxime

: 464-49-3,68546-28-1
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

: 26585-74-0
((R)-2,2,3-Trimethyl-cyclopent-3-enyl)-acetonitrile

: 113375-35-2
α-campholenic amide

: 113375-34-1
2,2-dimethyl-3-methylenecyclopentylacetonitrile

Conditions

Conditions	Yield
In methanol; at 20 - 30 ℃; for 15h; Further byproducts given. Yields of byproduct given; Irradiation;	32%

: 2792-42-9
(R,R)-camphor oxime

: 464-49-3,68546-28-1
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

: 26585-74-0
((R)-2,2,3-Trimethyl-cyclopent-3-enyl)-acetonitrile

: 113375-34-1
2,2-dimethyl-3-methylenecyclopentylacetonitrile

: 108268-00-4
1,8,8-trimethyl-2-azabicyclo<3.2.1>octan-3-one