Welcome to LookChem.com Sign In|Join Free

CAS

  • or

64701-47-9

Post Buying Request

64701-47-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

64701-47-9 Usage

Uses

1-Pyrenedecanoic acid is an anionic membrane probe.

Check Digit Verification of cas no

The CAS Registry Mumber 64701-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,0 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64701-47:
(7*6)+(6*4)+(5*7)+(4*0)+(3*1)+(2*4)+(1*7)=119
119 % 10 = 9
So 64701-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C26H28O2/c27-24(28)12-7-5-3-1-2-4-6-9-19-13-14-22-16-15-20-10-8-11-21-17-18-23(19)26(22)25(20)21/h8,10-11,13-18H,1-7,9,12H2,(H,27,28)

64701-47-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Sigma

  • (82660)  1-Pyrenedecanoic acid  suitable for fluorescence, ≥98.0% (HPLC)

  • 64701-47-9

  • 82660-25MG

  • 3,416.40CNY

  • Detail

64701-47-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-PYRENEDECANOIC ACID

1.2 Other means of identification

Product number -
Other names Pyrendecan-saeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64701-47-9 SDS

64701-47-9Synthetic route

pyrenoylnonanoic acid methyl ester
228243-58-1

pyrenoylnonanoic acid methyl ester

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Conditions
ConditionsYield
With potassium hydroxide; hydrazine hydrate In ethylene glycol Kischner-Wolf reaction;89%
1-(9-carbethoxy-1-oxononanyl)pyrene
70700-34-4

1-(9-carbethoxy-1-oxononanyl)pyrene

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Conditions
ConditionsYield
With potassium hydroxide; hydrazine hydrate In diethylene glycol at 162 - 178℃; for 4h;86%
pyrene
129-00-0

pyrene

monoethyl sebacate
693-55-0

monoethyl sebacate

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Conditions
ConditionsYield
2.) Wolf-Kischner reduction; Multistep reaction;
3,5-Dinitro-benzoic acid (E)-(15R,16S)-15,17-dihydroxy-16-(10-pyren-1-yl-decanoylamino)-heptadec-13-enyl ester
448210-97-7

3,5-Dinitro-benzoic acid (E)-(15R,16S)-15,17-dihydroxy-16-(10-pyren-1-yl-decanoylamino)-heptadec-13-enyl ester

A

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

B

(4E,2S,3R)-2-amino-1,3,17-trihydroxy-17-(3,5-dinitrobenzoyl)-4-heptadecene
448211-01-6

(4E,2S,3R)-2-amino-1,3,17-trihydroxy-17-(3,5-dinitrobenzoyl)-4-heptadecene

Conditions
ConditionsYield
With ceramidase from Pseudomonas aeruginosa PA01; calcium chloride; Triton X-100 In water at 30℃; for 0.333333h; pH=8.5; Enzyme kinetics; Further Variations:; pH-values; Reagents;
methyl 10-chloro-10-oxodecanoate
14065-32-8

methyl 10-chloro-10-oxodecanoate

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 48.9 percent / AlCl3 / CH2Cl2
2: 89 percent / hydrazine hydrate; KOH / ethane-1,2-diol
View Scheme
sebacic acid mono methyl ester
818-88-2

sebacic acid mono methyl ester

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: oxalyl chloride
2: 48.9 percent / AlCl3 / CH2Cl2
3: 89 percent / hydrazine hydrate; KOH / ethane-1,2-diol
View Scheme
1,10-decanedioic acid
111-20-6

1,10-decanedioic acid

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 82 percent / diethyl sebacate, HCl / dibutyl ether
2: 93 percent / thionyl chloride / petroleum ether
3: 62 percent / AlCl3 / CS2 / 1.) 0 deg C, 1 h, 2.) 25 deg C, 11 h
4: 86 percent / potassium hydroxide, hydrazine hydrate / bis-(2-hydroxy-ethyl) ether / 4 h / 162 - 178 °C
View Scheme
monoethyl sebacate
693-55-0

monoethyl sebacate

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 93 percent / thionyl chloride / petroleum ether
2: 62 percent / AlCl3 / CS2 / 1.) 0 deg C, 1 h, 2.) 25 deg C, 11 h
3: 86 percent / potassium hydroxide, hydrazine hydrate / bis-(2-hydroxy-ethyl) ether / 4 h / 162 - 178 °C
View Scheme
9-ethoxycarbonylnonanoic acid chloride
6946-46-9

9-ethoxycarbonylnonanoic acid chloride

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 62 percent / AlCl3 / CS2 / 1.) 0 deg C, 1 h, 2.) 25 deg C, 11 h
2: 86 percent / potassium hydroxide, hydrazine hydrate / bis-(2-hydroxy-ethyl) ether / 4 h / 162 - 178 °C
View Scheme
4-nitro-phenol
100-02-7

4-nitro-phenol

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

10-(1-pyrenyl)decanoic acid p-nitrophenyl ester
228243-59-2

10-(1-pyrenyl)decanoic acid p-nitrophenyl ester

Conditions
ConditionsYield
With dicyclohexyl-carbodiimide In dichloromethane Esterification;94%
2,3,4,5,6-pentafluorophenol
771-61-9

2,3,4,5,6-pentafluorophenol

10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

10-(1-pyrenyl)decanoic acid pentafluorophenyl ester
228243-60-5

10-(1-pyrenyl)decanoic acid pentafluorophenyl ester

Conditions
ConditionsYield
With dicyclohexyl-carbodiimide In dichloromethane Esterification;91.9%
10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Pyrendecanoylchlorid
70796-35-9

Pyrendecanoylchlorid

Conditions
ConditionsYield
With thionyl chloride In Petroleum ether at 40 - 60℃; for 9h;
10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

3-O-benzoyl-2-N-(4-(1-pyrenyl)decanoyl)-D,L-erythro-sphinganine

3-O-benzoyl-2-N-(4-(1-pyrenyl)decanoyl)-D,L-erythro-sphinganine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 94 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 55.1 percent / pyridine; Et3N / 5 h / 20 °C
View Scheme
Multi-step reaction with 2 steps
1: 91.9 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 49 percent / pyridine / 20 °C
View Scheme
10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

3-O-benzoyl-2-N-(4-(1-pyrenyl)decanoyl)-D,L-erythro-sphinganine-1-O-(N,N-diisopropylamino)-2-cyanoethylphosphine

3-O-benzoyl-2-N-(4-(1-pyrenyl)decanoyl)-D,L-erythro-sphinganine-1-O-(N,N-diisopropylamino)-2-cyanoethylphosphine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 94 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 55.1 percent / pyridine; Et3N / 5 h / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
View Scheme
Multi-step reaction with 3 steps
1: 91.9 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 49 percent / pyridine / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
View Scheme
10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

2-N-(4-(1-pyrenyl)decanoyl)-D,L-erythro-sphinganine-1-O-phospho-5'-thymidine

2-N-(4-(1-pyrenyl)decanoyl)-D,L-erythro-sphinganine-1-O-phospho-5'-thymidine

Conditions
ConditionsYield
Multi-step reaction with 7 steps
1: 94 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 55.1 percent / pyridine; Et3N / 5 h / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
4: 1H-tetrazole / CH2Cl2; acetonitrile / 0.5 h / 20 °C
5: tert-butyl hydroperoxide / CH2Cl2; acetonitrile / 0.67 h
6: 54.5 percent / toluene / 4 h / 20 °C
7: 89.9 percent / 0.2 N MeONa / diethyl ether; methanol / 1 h / 20 °C
View Scheme
Multi-step reaction with 7 steps
1: 91.9 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 49 percent / pyridine / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
4: 1H-tetrazole / CH2Cl2; acetonitrile / 0.5 h / 20 °C
5: tert-butyl hydroperoxide / CH2Cl2; acetonitrile / 0.67 h
6: 54.5 percent / toluene / 4 h / 20 °C
7: 89.9 percent / 0.2 N MeONa / diethyl ether; methanol / 1 h / 20 °C
View Scheme
10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Benzoic acid 1-[2-[[(2R,3S,5R)-3-acetoxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethoxy]-(2-cyano-ethoxy)-phosphanyloxy]-1-(10-pyren-1-yl-decanoylamino)-ethyl]-hexadecyl ester

Benzoic acid 1-[2-[[(2R,3S,5R)-3-acetoxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethoxy]-(2-cyano-ethoxy)-phosphanyloxy]-1-(10-pyren-1-yl-decanoylamino)-ethyl]-hexadecyl ester

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 94 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 55.1 percent / pyridine; Et3N / 5 h / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
4: 1H-tetrazole / CH2Cl2; acetonitrile / 0.5 h / 20 °C
View Scheme
Multi-step reaction with 4 steps
1: 91.9 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 49 percent / pyridine / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
4: 1H-tetrazole / CH2Cl2; acetonitrile / 0.5 h / 20 °C
View Scheme
10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

Benzoic acid 1-[2-[[(2R,3S,5R)-3-acetoxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethoxy]-(2-cyano-ethoxy)-phosphoryloxy]-1-(10-pyren-1-yl-decanoylamino)-ethyl]-hexadecyl ester

Benzoic acid 1-[2-[[(2R,3S,5R)-3-acetoxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethoxy]-(2-cyano-ethoxy)-phosphoryloxy]-1-(10-pyren-1-yl-decanoylamino)-ethyl]-hexadecyl ester

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: 94 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 55.1 percent / pyridine; Et3N / 5 h / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
4: 1H-tetrazole / CH2Cl2; acetonitrile / 0.5 h / 20 °C
5: tert-butyl hydroperoxide / CH2Cl2; acetonitrile / 0.67 h
View Scheme
Multi-step reaction with 5 steps
1: 91.9 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 49 percent / pyridine / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
4: 1H-tetrazole / CH2Cl2; acetonitrile / 0.5 h / 20 °C
5: tert-butyl hydroperoxide / CH2Cl2; acetonitrile / 0.67 h
View Scheme
10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

3-O-benzoyl-2-N-(4-(1-pyrenyl)decanoyl)-D,L-erythro-sphinganine-1-O-phospho-5'-(3'-O-acetyl)thymidine triethylammonium salt

3-O-benzoyl-2-N-(4-(1-pyrenyl)decanoyl)-D,L-erythro-sphinganine-1-O-phospho-5'-(3'-O-acetyl)thymidine triethylammonium salt

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1: 94 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 55.1 percent / pyridine; Et3N / 5 h / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
4: 1H-tetrazole / CH2Cl2; acetonitrile / 0.5 h / 20 °C
5: tert-butyl hydroperoxide / CH2Cl2; acetonitrile / 0.67 h
6: 54.5 percent / toluene / 4 h / 20 °C
View Scheme
Multi-step reaction with 6 steps
1: 91.9 percent / dicyclohexylcarbodiimide / CH2Cl2
2: 49 percent / pyridine / 20 °C
3: 75.9 percent / diisopropylammonium tetrazolide / CH2Cl2; acetonitrile
4: 1H-tetrazole / CH2Cl2; acetonitrile / 0.5 h / 20 °C
5: tert-butyl hydroperoxide / CH2Cl2; acetonitrile / 0.67 h
6: 54.5 percent / toluene / 4 h / 20 °C
View Scheme
10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

ethyl ω-(1-pyreno)decanoate
73116-44-6

ethyl ω-(1-pyreno)decanoate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: SOCl2 / petroleum ether / 9 h / 40 - 60 °C
2: petroleum ether
View Scheme
10-(1-pyrenyl)decanoic acid
64701-47-9

10-(1-pyrenyl)decanoic acid

C10H24O3Si

C10H24O3Si

C36H50O4Si

C36H50O4Si

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane

64701-47-9Relevant articles and documents

New Fluorescence from Molecular Aggregates of 10-(1-pyrenyl)decanoic Acid

Itaya, Akira,Kawamura, Tsuneo,Masuhara, Hiroshi,Taniguchi, Yoshio,Mitsuya, Munehisa,et al.

, p. 1541 - 1544 (1986)

In addition to the normal monomer and excimer fluorescence, vacuum-deposited, cast and their laser-irradiated films of 10-(1-pyrenyl)decanoic acid showed three kinds of fluorescence bands.Similar new fluorescence bands were also observed in its aqueous solution.These emissions were due to meta-stable aggregates of pyrenyl chromophores whose structures were ascribed to molecular interactions operating during the processes of film preparation.

Synthesis and intermembrane transfer of pyrene-labelled liponucleotides: Ceramide phosphothymidines

Oskolkova, Olga V.,Shvets, Vitaly I.,Hermetter, Albin,Paltauf, Fritz

, p. 73 - 86 (2007/10/03)

Phospholipid conjugates of 3'-azido-3'-deoxythymidine (AZT) show activity against human immunodeficiency virus (HIV) in vitro. Here we report on the synthesis and characterization of two pyrene containing conjugates: 2-N-(4-(pyren-1-yl)butanoyl)ceramide 5'-phosphothymidine (Pbs-Cer-P-T) (XII) and 2-N-(10-(pyren-1-yl)decanoyl)ceramide 5'-phosphothymidine (Pds-Cer-P-T) (XIII). These fluorescent labelled conjugates served as model compounds to study incorporation of sphingoliponucleotides into membranes. The complex compounds were prepared by condensation of 3'-acetylthymidine and labelled ceramides using the phosphite triester coupling procedure. UV absorption, fluorimetry as well as 1H-, 31P-, 13C-NMR analyses were used for structure confirmation of the synthesized substances. When incorporated into small unilamellar 1-palmitoyl-2-oleoyl-glycerophosphatidylcholine (POPC) vesicles and incubated with unlabelled acceptor POPC vesicles, the compounds (XII) and (XIII) exhibited spontaneous transfer. Kinetic data suggest that transfer from donor to acceptor vesicles occurred via the intervening aqueous phase. The non-specific lipid transfer protein from bovine liver stimulated the transfer of Pds-Cer-P-T between phospholipid vesicles in a concentration dependent manner. Copyright (C) 1999 Elsevier Science Ireland Ltd.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 64701-47-9