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[ CAS No. 29882-07-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 29882-07-3
Chemical Structure| 29882-07-3
Structure of 29882-07-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 29882-07-3 ]

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Product Citations

Product Details of [ 29882-07-3 ]

CAS No. :29882-07-3 MDL No. :MFCD09032953
Formula : C6H13ClO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :LTLKJYMNUSSFAH-UHFFFAOYSA-N
M.W : 152.62 Pubchem ID :122536
Synonyms :

Calculated chemistry of [ 29882-07-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 5
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 37.92
TPSA : 18.46 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.18
Log Po/w (XLOGP3) : 1.4
Log Po/w (WLOGP) : 1.62
Log Po/w (MLOGP) : 1.36
Log Po/w (SILICOS-IT) : 1.52
Consensus Log Po/w : 1.62

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.34
Solubility : 7.0 mg/ml ; 0.0459 mol/l
Class : Very soluble
Log S (Ali) : -1.39
Solubility : 6.19 mg/ml ; 0.0406 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.0
Solubility : 1.54 mg/ml ; 0.0101 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.2

Safety of [ 29882-07-3 ]

Signal Word:Danger Class:3
Precautionary Statements:P501-P240-P210-P233-P243-P241-P242-P264-P280-P370+P378-P337+P313-P305+P351+P338-P362+P364-P303+P361+P353-P332+P313-P403+P235 UN#:1993
Hazard Statements:H315-H319-H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 29882-07-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 29882-07-3 ]

[ 29882-07-3 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 681-84-5 ]
  • [ 4635-59-0 ]
  • [ 29882-07-3 ]
  • 2
  • [ 4635-59-0 ]
  • [ 149-73-5 ]
  • [ 29882-07-3 ]
  • 3
  • [ 29882-07-3 ]
  • [ 107-02-8 ]
  • [ 29882-08-4 ]
  • 4
  • [ 67-56-1 ]
  • [ 1489-69-6 ]
  • [ 29882-07-3 ]
  • 6
  • [ 29882-07-3 ]
  • [ 2863-98-1 ]
  • [ 46276-24-8 ]
  • 7
  • [ 29882-07-3 ]
  • [ 40566-85-6 ]
  • [ 7272-54-0 ]
YieldReaction ConditionsOperation in experiment
In ethanol; water; b. 2-(5-Carboethoxy-1H-indol-3-yl)ethylamine A solution of ethyl-p-hydrazinobenzoate hydrochloride (10 g, 46 mmol) and <strong>[29882-07-3]4-chlorobutanal dimethyl acetal</strong> (7.8 g, 46 mmol) in ethanol/water (5:1, 500 ml) was heated at reflux for 2 hours. The solvent was removed under vacuum and the residue chromatographed through silica gel eluding with dichloromethane/ethanol/ammonia (40:8:1) to give the title indole (3.69 g) as an oil. NMR delta (360 MHz, CDCl3) 1.42 (3H, t, J=7 Hz), 2.94 (2H, t, J=7 Hz), 3.06 (2H, t, J=7 Hz), 4.40 (2H, q, J=7 Hz), 7.10 (1H, br s), 7.35 (1H, d, J=9 Hz), 7.91 (1H, dd, J=9 and 2 Hz), 8.30 (1H, br s), 8.38 (1H, s).
  • 8
  • [ 29882-07-3 ]
  • 4-Hydrazinobenzeneacetonitrile hydrochloride [ No CAS ]
  • [ 148458-97-3 ]
YieldReaction ConditionsOperation in experiment
In methanol; ethanol; water; 2. 2-(5-Cyanomethyl-1H-indol-3-yl)ethylamine. Hydrochloride 4-Chlorobutanal dimethylacetal (37.07 g, 0.24 mol) was added to a stirred solution of 4-hydrazinobenzyl cyanide hydrochloride (47.0 g, 0.26 mol) in EtOH/H2 O (5:1; 21) and refluxed for 4.5 h. The reaction mixture was evaporated to dryness under vacuum, MeOH (150 ml) added, and the mixture left at 0° C. for 10 h. The resultant pale yellow precipitate was filtered under vacuum, washed with Et2 O/MeOH (5:1; 2*100 ml) and dried. The product was used without further purification (24.1 g, 40percent), m.p. 239°-241° C.; Rf 0.4 in CH2 Cl2 /EtOH/NH3 (40:8:1); 1 H NMR (360 MHz, D2 O) 3.18 (2H, t, J=7.1 Hz, CH2); 3.36 (2H, t, J=7.1 Hz, CH2); 4.02 (2H, s, CH2); 7.22 (1H, dd, J=1.5and 8.4 Hz, Ar-H); 7.36 (1H, s, Ar-H); 7.56 (1H, d, J=8.4 Hz, Ar-H); 7.66 (1H, s, Ar-H).
  • 9
  • [ 29882-07-3 ]
  • 4-(ethoxycarbonylmethyl)phenyl hydrazine hydrochloride [ No CAS ]
  • [ 137499-22-0 ]
  • 10
  • [ 29882-07-3 ]
  • 3-(4-Hydrazino-phenyl)-propionic acid ethyl ester; hydrochloride [ No CAS ]
  • [ 105324-00-3 ]
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