6H-Cyclopenta[b]furan-6-one, hexahydro-3a,6a-dihydroxy-, (3aR,6aR)-rel- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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Basic information
1. Product Name: 6H-Cyclopenta[b]furan-6-one, hexahydro-3a,6a-dihydroxy-, (3aR,6aR)-rel- (9CI)
2. Synonyms: 6H-Cyclopenta[b]furan-6-one, hexahydro-3a,6a-dihydroxy-, (3aR,6aR)-rel- (9CI)
3. CAS NO:587875-10-3
4. Molecular Formula: C7H10O4
5. Molecular Weight: 158.1519
6. EINECS: N/A
7. Product Categories: ALCOHOL
8. Mol File: 587875-10-3.mol
Chemical Properties
1. Melting Point: N/A
2. Boiling Point: N/A
3. Flash Point: N/A
4. Appearance: /
5. Density: N/A
6. Refractive Index: N/A
7. Storage Temp.: N/A
8. Solubility: N/A
9. CAS DataBase Reference: 6H-Cyclopenta[b]furan-6-one, hexahydro-3a,6a-dihydroxy-, (3aR,6aR)-rel- (9CI)(CAS DataBase Reference)
10. NIST Chemistry Reference: 6H-Cyclopenta[b]furan-6-one, hexahydro-3a,6a-dihydroxy-, (3aR,6aR)-rel- (9CI)(587875-10-3)
11. EPA Substance Registry System: 6H-Cyclopenta[b]furan-6-one, hexahydro-3a,6a-dihydroxy-, (3aR,6aR)-rel- (9CI)(587875-10-3)
Safety Data
1. Hazard Codes: N/A
2. Statements: N/A
3. Safety Statements: N/A
4. WGK Germany:
5. RTECS:
6. HazardClass: N/A
7. PackingGroup: N/A
8. Hazardous Substances Data: 587875-10-3(Hazardous Substances Data)

587875-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 587875-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,7,8,7 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 587875-10:
(8*5)+(7*8)+(6*7)+(5*8)+(4*7)+(3*5)+(2*1)+(1*0)=223
223 % 10 = 3
So 587875-10-3 is a valid CAS Registry Number.

587875-10-3Upstream product

587875-10-3Downstream Products

587875-10-3Relevant articles and documents

Asymmetric oxidation of 3-alkyl-1,2-cyclopentanediones. Part 3: Oxidative ring cleavage of 3-hydroxyethyl-1,2-cyclopentanediones: Synthesis of α-hydroxy-γ-lactone acids and spiro-γ-dilactones

Paju, Anne,Kanger, Tonis,Niitsoo, Olivia,Pehk, Tonis,Mueuerisepp, Aleksander-Mati,Lopp, Margus

, p. 2393 - 2399 (2007/10/03)

A Ti(OiPr)4/diethyl tartrate/tBuOOH complex oxidizes 3-hydroxyethyl-1,2-cyclopentanediones, resulting in hydroxylated/ring cleavage products - lactone acids of high enantioselectivity (up to 95% ee) with good yields (up to 75%). These compounds are converted into chiral spiro-γ-dilactones in good yield.

Asymmetric oxidation of 3-alkyl-1,2-cyclopentanediones. Part 1: 3-Hydroxylation of 3-alkyl-1,2-cyclopentanediones

Paju, Anne,Kanger, Tonis,Pehk, Tonis,Mueuerisepp, Aleksander-Mati,Lopp, Margus

, p. 2439 - 2448 (2007/10/03)

3-Alkyl-1,2-cyclopentanediones undergo asymmetric 3-hydroxylation with the Sharpless Ti-complex resulting in enantiomeric 3-hydroxy carbonyl compounds with ee up to 95% in yields of 22-40%.

Asymmetric oxidation of 1,2-cyclopentanediones

Paju, Anne,Kanger, T?nis,Pehk, T?nis,Lopp, Margus

, p. 6883 - 6887 (2007/10/03)

Cyclic 3-alkyl-1,2-cyclopentanediones undergo a direct asymmetric oxidation with the DET/Ti(OiPr)4/ tBuOOH oxidative system, resulting in enantiomeric α-hydroxy compounds and ring-cleaved hydroxylated acids (lactones) up to 95% ee. (C) 2000 Elsevier Science Ltd.

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CAS

587875-10-3