16326-98-0

Basic information

• Product Name: 1,3-Cyclopentanediol, (1R,3R)-rel-
• CAS NO: 16326-98-0
• Molecular Formula: C5H10O2
• Molecular Weight: 102.133
• Mol File: 16326-98-0.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: 1,3-Cyclopentanediol, (1R,3R)-rel-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Cyclopentanediol, (1R,3R)-rel-(16326-98-0)
• EPA Substance Registry System: 1,3-Cyclopentanediol, (1R,3R)-rel-(16326-98-0)

Safety Data

• Hazardous Substances Data: 16326-98-0(Hazardous Substances Data)

Usage

Explanation

1,3-Cyclopentanediol, (1R,3R)-relis composed of 5 carbon atoms, 10 hydrogen atoms, and 2 oxygen atoms.

Explanation

The compound has a chiral center, which means it has a non-superimposable mirror image (enantiomer). This is due to the presence of two hydroxyl groups attached to adjacent carbon atoms in a cyclopentane ring.

Explanation

The compound has a five-membered carbon ring structure, which is a cyclopentane.

Explanation

The stereochemistry of the compound is defined by the (1R,3R)-configuration, which indicates the spatial arrangement of the hydroxyl groups on the cyclopentane ring.

Explanation

1,3-Cyclopentanediol, (1R,3R)-relis used as a chiral building block in the synthesis of pharmaceuticals and other complex molecules.

Explanation

1,3-Cyclopentanediol, (1R,3R)-relis also utilized as a reagent in chemical research and development processes.

Chiral Compound

Yes

Cyclopentane Ring

Present

Hydroxyl Groups

Two

Stereochemistry

(1R,3R)-rel-

Application

Organic Synthesis

Asymmetric Synthesis

Valuable

Use as a Reagent

Chemical Research and Development

Upstream product

• 7129-41-1 6-oxabicyclo[3.1.0]hex-2-ene 
• 5870-62-2 3-hydroxy-2-cyclopenten-1-one 
• 98-00-0 (2-furyl)methyl alcohol 
• 59995-47-0 4-Hydroxycyclopent-2-enone 
• 3859-41-4 1,3-cyclopentadione 
• 542-92-7 cyclopenta-1,3-diene 
• 16326-97-9 1,3-dihydroxycyclopentane 
• 279-35-6 1,3-epiperoxycyclopentane 
• 603-35-0 triphenylphosphine 
• 98-01-1 furfural 

Downstream Products

• 16326-97-9 trans-1,3-cyclopentanediol 
• 874650-39-2 3-hydroxycyclopentyl 4-methylbenzenesulfonate 
• 247568-60-1 3-hydroxycyclopentyl benzoate 
• 109905-54-6 (S)-3-hydroxycyclopentanone 
• 77-73-6 bi(cyclopentadiene) 
• 542-92-7 cyclopenta-1,3-diene 
• 77-73-6 dicyclopentadiene 
• 2825-83-4 (3aR,4R,7S,7aS)-octahydro-1H-4,7-methanoindene 
• 142-29-0 cyclopentene 
• 14320-38-8 cyclopent-3-enol 
• 2825-83-4 (3aR,4S,7R,7aS)-Octahydro-4,7-methano-indene 
• 1755-01-7 endo-Dicyclopentadien 
• 247568-63-4 2-[3-(Benzoyloxy)cyclopentylamino]-N-benzyl-5-nitrobenzamide 
• 247568-61-2 3-azidocyclopentyl benzoate 

Relevant articles and documents

Interaction of Triphenylphosphine with 2,3-Dioxabicycloheptane

The reaction of triphenylphosphine with 2,3-dioxabicycloheptane resulted in the formation of a phosphorane that decomposed in the presence of water to give triphenylphosphine oxide and trans-1,3-cyclopentanediol.

Application of hierarchical pore molecular sieve in preparation process of cyclopentadiene and JP-10 aviation fuel

The invention relates to an application of a hierarchical pore molecular sieve in a the preparation process of cyclopentadiene and JP-10 aviation fuel. The hierarchical pore molecular sieve is one or two or more of an H-ZSM-5 molecular sieve, an H-beta molecular sieve, an H-Y molecular sieve, an H-USY molecular sieve, a La-Y molecular sieve and an H-MOR molecular sieve with a hierarchical pore structure, a sulfonated SBA-15 molecular sieve, a sulfonated MCM-41 molecular sieve, a sulfonated Ti-SBA-15 molecular sieve, a sulfonated MCM-41 molecular sieve, a sulfonated Zr-MCM-41 molecular sieve and a sulfonated Zr-SBA-15 molecular sieve; and the hierarchical pore structure comprises micropores and mesopores. The catalyst and the raw materials used in the method are cheap and easy to obtain, the preparation process is simple, and the hierarchical pore molecular sieve has high activity and selectivity for rearrangement reaction of furfuryl alcohol, hydrogenation reaction of hydroxyl cyclopentenone and dehydration reaction. The invention provides a cheap and efficient synthesis method for synthesizing the JP-10 aviation fuel from a lignocellulose-based platform compound furfuryl alcohol.

Making JP-10 Superfuel Affordable with a Lignocellulosic Platform Compound

The synthesis of renewable jet fuel from lignocellulosic platform compounds has drawn a lot of attention in recent years. So far, most work has concentrated on the production of conventional jet fuels. JP-10 is an advanced jet fuel currently obtained from fossil energy. Due to its excellent properties, JP-10 has been widely used in military aircraft. However, the high price and low availability limit its application in civil aviation. Here, we report a new strategy for the synthesis of bio-JP-10 fuel from furfuryl alcohol that is produced on an industrial scale from agricultural and forestry residues. Under the optimized conditions, bio-JP-10 fuel was produced with high overall carbon yields (≈65 %). A preliminary economic analysis indicates that the price of bio-JP-10 fuel can be greatly decreased from ≈7091 US$/ton (by fossil route) to less than 5600 US$/ton using our new strategy. This work makes the practical application of bio-JP-10 fuel forseeable.