25501-32-0

  • Product Name:(S)-(+)-1-Indanol
Inquiry

Product Details

Purity:99%

25501-32-0 In Stock, (S)-(+)-1-Indanol Fast Delivery

  • Molecular Formula:C9H10 O
  • Molecular Weight:134.178
  • Vapor Pressure:0.00859mmHg at 25°C 
  • Melting Point:69-73oC 
  • Boiling Point:255.1ºC at 760 mmHg 
  • PKA:14.23±0.20(Predicted) 
  • Flash Point:89.2ºC 
  • PSA:20.23000 
  • Density:1.161g/cm3 
  • LogP:1.66620 

(S)-(+)-1-Indanol(Cas 25501-32-0) Usage

Uses

(S)-(+)-1-Indanol is a building block used in pharmaceutical synthesis such as orally bioavailable GPR40 agonists such as DS-1558 used to stimulate insulin secretion.

InChI:InChI=1/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2/t9-/m0/s1

25501-32-0 Relevant articles

Asymmetric transfer hydrogenation of ketonic substrates catalyzed by (η5-C5Me5)MCl complexes (M = Rh and Ir) of (1S, 2S)-N-(p-toluenesulfonyl)-1,2-diphenylethylenediamine

Mashima, Kazushi,Abe, Tomoyuki,Tani, Kazuhide

, p. 1199 - 1200 (1998)

The rhodium and iridium (η5-C5Me5)MCl co...

Asymmetric Aggregative Activation. A New Useful Concept for Asymmetric Reduction

Lalloz, Lucien,Vanderesse, Regis,Mayesky, Bertrand,Caubere, Paul

, p. 1961 - 1964 (1991)

Reduction of arylketones with a Complex ...

Designer Outer Membrane Protein Facilitates Uptake of Decoy Molecules into a Cytochrome P450BM3-Based Whole-Cell Biocatalyst

Karasawa, Masayuki,Shoji, Osami,Stanfield, Joshua Kyle,Suzuki, Kazuto,Yonemura, Kai

supporting information, (2021/12/16)

We report an OmpF loop deletion mutant, ...

Dynamic Kinetic Resolution of Alcohols by Enantioselective Silylation Enabled by Two Orthogonal Transition-Metal Catalysts

Oestreich, Martin,Seliger, Jan

, p. 247 - 251 (2020/10/29)

A nonenzymatic dynamic kinetic resolutio...

Homochiral Dodecanuclear Lanthanide "cage in Cage" for Enantioselective Separation

Zhu, Chengfeng,Tang, Haitong,Yang, Keke,Fang, Yu,Wang, Kun-Yu,Xiao, Zhifeng,Wu, Xiang,Li, Yougui,Powell, Joshua A.,Zhou, Hong-Cai

supporting information, p. 12560 - 12566 (2021/08/23)

It is extremely difficult to anticipate ...

Cobalt-catalyzed asymmetric hydrogenation of ketones: A remarkable additive effect on enantioselectivity

Du, Tian,Wang, Biwen,Wang, Chao,Xiao, Jianliang,Tang, Weijun

supporting information, p. 1241 - 1244 (2020/10/02)

A chiral cobalt pincer complex, when com...

25501-32-0 Process route

Isopropenyl acetate
108-22-5

Isopropenyl acetate

1-Indanol
6351-10-6

1-Indanol

2,3-dihydro-1H-inden-1-yl-acetate
26452-98-2

2,3-dihydro-1H-inden-1-yl-acetate

(S)-indanol
25501-32-0

(S)-indanol

Conditions
Conditions Yield
With lipase from Pseudomonas cepacia immobilized on ceramic; In toluene; at 40 ℃; for 4h;
 
1-Indanol
6351-10-6

1-Indanol

(S)-indanol
25501-32-0

(S)-indanol

Conditions
Conditions Yield
With dichloro(norbornadiene)palladium(II); oxygen; (-)-sparteine; 3 A molecular sieve; In toluene; at 60 ℃; for 54h; under 760.051 Torr;
25%
 
 
Multi-step reaction with 3 steps
1: 78 percent / 4-DMAP; pyridine / tetrahydrofuran / 2 h / 20 °C
2: Candida antarctica B lipase; n-butanol / acetonitrile / 192 h
3: aq. LiOH / methanol / 3 h / Heating
With pyridine; dmap; lithium hydroxide; Candida antarctica B lipase; butan-1-ol; In tetrahydrofuran; methanol; acetonitrile;
 
Multi-step reaction with 2 steps
1: t-BuOK / (CyRuCl2)2; (1R,2S)-(+)-cis-1-aminoindan-2-ol / propan-2-ol; acetone / 1 h / 25 °C
2: t-BuOK / (CyOsCl2)2; (1R,2S)-(+)-cis-1-aminoindan-2-ol / propan-2-ol / 48 h / -24 °C
With potassium tert-butylate; (CyOsCl2)2; (CyRuCl2)2; (1R,2S)-1-Amino-2-indanol; In isopropyl alcohol; acetone;
 
Multi-step reaction with 3 steps
1: Py
2: cinchonidine
3: aq. KOH / methanol
With pyridine; potassium hydroxide; Cinchonidin; In methanol;
 
Multi-step reaction with 2 steps
1: Py
2: aq. KOH / methanol
With pyridine; potassium hydroxide; In methanol;
 
Multi-step reaction with 2 steps
1: dmap / dichloromethane / 4 h / 20 °C
2: Candida rugosa lipase / tetrahydrofuran; aq. phosphate buffer / 24 h / 30 °C / pH 7 / Resolution of racemate; Enzymatic reaction
With dmap; Candida rugosa lipase; In tetrahydrofuran; aq. phosphate buffer; dichloromethane;
 
Multi-step reaction with 2 steps
1: (R,R)-N-(1-(β-1-naphthyl)ethyl)benzoguanidine; N-ethyl-N,N-diisopropylamine / toluene / 24 h / -78 °C / Inert atmosphere
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere
With (R,R)-N-(1-(β-1-naphthyl)ethyl)benzoguanidine; tetrabutyl ammonium fluoride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; toluene;
 
Multi-step reaction with 2 steps
1: N-ethyl-N,N-diisopropylamine; C23H21N3 / toluene / 24 h / -78 °C / Inert atmosphere
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C / Inert atmosphere
With C23H21N3; tetrabutyl ammonium fluoride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; toluene;
 
With 6C26H22N2O6(2-)*3C10H8N2*8Zn(2+)*2O(2-); In acetone; at 20 ℃; enantioselective reaction;
99.3 % ee
Multi-step reaction with 2 steps
1: oxygen; dipropylene glycol dimethyl ether / 120 °C
2: C31H36N2O2RuS; sodium formate / methanol; water / 12 h / 50 °C / Inert atmosphere
With dipropylene glycol dimethyl ether; oxygen; sodium formate; C31H36N2O2RuS; In methanol; water;
 
Multi-step reaction with 2 steps
1: (OC-6-23)-[2-[6-[(amino-κN)methyl]-2-pyridinyl-κN]-5-methylphenyl-κC][1,1'-(1,4-butanediyl)bis[1,1-diphenylphosphine-κP]]chlororuthenium(II); copper(l) chloride; sodium t-butanolate; (R,R)-1,2-bis(2,5-diphenylphospholanyl)ethane / toluene / 14 h / 20 °C / Glovebox; Inert atmosphere
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere
With (OC-6-23)-[2-[6-[(amino-κN)methyl]-2-pyridinyl-κN]-5-methylphenyl-κC][1,1'-(1,4-butanediyl)bis[1,1-diphenylphosphine-κP]]chlororuthenium(II); tetrabutyl ammonium fluoride; copper(l) chloride; sodium t-butanolate; (R,R)-1,2-bis(2,5-diphenylphospholanyl)ethane; In tetrahydrofuran; toluene;
 
1-Indanol; With (Δ)12-PCC-57; In acetone; at 20 ℃; for 8h;
In dichloromethane; enantioselective reaction;
99.7 % ee

25501-32-0 Upstream products

  • 83-33-0
    83-33-0

    inden-1-one

  • 108-22-5
    108-22-5

    Isopropenyl acetate

  • 6351-10-6
    6351-10-6

    1-Indanol

  • 100465-50-7
    100465-50-7

    <1,1'-Binaphthalene>-2,2'-diol dibutanoate

25501-32-0 Downstream products

  • 175288-46-7
    175288-46-7

    [2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-isopropyl-carbamic acid (S)-indan-1-yl ester

  • 83-33-0
    83-33-0

    inden-1-one

  • 256237-45-3
    256237-45-3

    (S)-N,N-diisopropyl O-(indan-1-yl)carbamate

  • 415975-55-2
    415975-55-2

    (2S,2R')-(3,4-dichlorophenyl)(tetrahydropyran-2-yl)acetic acid indanyl ester