Details
Reputable factory supply HOMOPIPERONYLAMINE 1484-85-1 in bulk at low price
- Molecular Formula: C9H11NO2
- Molecular Weight: 165.192
- Appearance/Colour: Colourless Liquid
- Vapor Pressure: 0.000618mmHg at 25°C
- Melting Point: 114 °C
- Refractive Index: 1.561
- Boiling Point: 274.3 ºCat 760 mmHg
- PKA: 9.90±0.10(Predicted)
- Flash Point: 129.8 ºC
- PSA： 44.48000
- Density: 1.204 g/c3
- LogP: 1.61680
HOMOPIPERONYLAMINE(Cas 1484-85-1) Usage
InChI:InChI=1/C10H13NO3/c1-12-8-4-7(2-3-11)5-9-10(8)14-6-13-9/h4-5H,2-3,6,11H2,1H3
1484-85-1 Relevant articles
-
Reeve,Eareckson
, p. 3299 (1950)
-
-
Gensler,Samour
, p. 5555 (1951)
-
-
Erne,Ramirez
, p. 912,915 (1950)
-
SYNTHESES BASED ON β-PHENYLETHYLAMINES. I. PREPARATION OF SUBSTITUTED β-PHENYLETHYLAMINES
Vinogradova, V. I.,Yunusov, M. S.,Kuchin, A. V.,Tolstikov, G. A.,Sagandykov, R. T.,et al.
, p. 54 - 59 (1990)
A comparative study has been made of met...
Structure–activity relationship and biological evaluation of berberine derivatives as PCSK9 down-regulating agents
Fan, Tian-Yun,Yang, Yu-Xin,Zeng, Qing-Xuan,Wang, Xue-Lei,Wei, Wei,Guo, Xi-Xi,Zhao, Li-Ping,Song, Dan-Qing,Wang, Yan-Xiang,Wang, Li,Hong, Bin
, (2021/06/01)
Proprotein convertase subtilisin/kexin t...
A method of synthesis of piperonolamine
-
Paragraph 0112; 0125-0127; 0128; 0141-0143; 0157; ..., (2022/01/07)
The present invention belongs to the fie...
A synthetic preparation method for small carbags hydrochloric acid
-
Paragraph 0200-0202, (2021/12/08)
The present invention belongs to the fie...
Enantioselective synthesis and anti-parasitic properties of aporphine natural products
Amaral, Maiara,Anderson, Edward A.,McHugh, Eliza,Pieper, Pauline,Tempone, Andre G.
, (2019/12/09)
Chagas disease and visceral leishmaniasi...
1484-85-1 Process route
-
-
1485-00-3,22568-48-5
5-((E)-2-nitroethenyl)-1,3-benzodioxole
-
-
1484-85-1
3,4-methylenedioxyphenylethylamine
| Conditions | Yield |
|---|---|
|
With
lithium aluminium tetrahydride;
In
tetrahydrofuran; diethyl ether;
at 0 - 70 ℃;
for 12h;
Inert atmosphere;
|
95%
|
|
With
lithium aluminium tetrahydride;
In
tetrahydrofuran;
Reflux;
|
87%
|
|
With
lithium aluminium tetrahydride;
In
tetrahydrofuran;
at 0 ℃;
Reflux;
|
84%
|
|
With
lithium aluminium tetrahydride;
In
tetrahydrofuran;
for 8h;
Heating;
|
72%
|
|
With
sodium tetrahydroborate; boron trifluoride diethyl etherate;
In
tetrahydrofuran;
for 6.5h;
Inert atmosphere;
Reflux;
|
66%
|
|
With
lithium aluminium tetrahydride;
In
tetrahydrofuran;
at 65 ℃;
for 6h;
|
|
|
With
lithium aluminium tetrahydride;
|
-
![3-(benzo[d][1,3]dioxol-5-yl)propanamide](/upload/2026/11/b04737c7e0414f3fabc9ee5f6c07d689_8cabad20-5689-4b9a-aa45-9502d11a4c22.png)
-
20799-84-2
3-(benzo[d][1,3]dioxol-5-yl)propanamide
-
-
1484-85-1
3,4-methylenedioxyphenylethylamine
| Conditions | Yield |
|---|---|
|
With
chlorine; sodium hydroxide;
In
water;
at -5 - 40 ℃;
for 4h;
Reagent/catalyst;
Temperature;
|
91%
|
|
With
chlorine; sodium hydroxide;
at 30 - 75 ℃;
for 2h;
Green chemistry;
|
90%
|
|
With
sodium hydroxide; bromine;
In
water;
at 70 - 80 ℃;
for 0.25h;
|
71%
|
|
With
sodium hypochlorite;
at 70 - 80 ℃;
|
1484-85-1 Upstream products
-
153361-93-4
benzo[1,3]dioxol-5-yl-acetaldehyde-oxime
-
20799-84-2
3-(benzo[d][1,3]dioxol-5-yl)propanamide
-
1485-00-3
5-(2-nitrovinyl)benzo[1,3]dioxole
-
119798-32-2
α-acetoxy-2-(3,4-methylenedioxyphenyl)acetonitrile
1484-85-1 Downstream products
-
855167-11-2
2-phenyl-quinoline-4-carboxylic acid-(2-benzo[1,3]dioxol-5-yl-ethylamide)
-
20341-12-2
N-(2-benzo[1,3]dioxol-5-ylethyl)-2-phenylacetamide
-
20341-16-6
N -(2-benzo[1,3]dioxol-5-yl-ethyl)-2-(3,4-dimethoxy-phenyl)-acetamide
-
494-55-3
N-methyl-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline
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