61367-41-7
- Product Name:trans-4-MethoxycyclohexanaMine HCl
- Molecular Formula:C7H15 N O . Cl H
- Purity:99%
- Molecular Weight:165.663
Product Details;
CasNo: 61367-41-7
Molecular Formula: C7H15 N O . Cl H
Factory Supply Hot Sale trans-4-MethoxycyclohexanaMine HCl 61367-41-7 Fast Shipping
- Molecular Formula:C7H15 N O . Cl H
- Molecular Weight:165.663
- Melting Point:199-200°C
- Boiling Point:174.5°Cat760mmHg
- Flash Point:53.1°C
- PSA:35.25000
- Density:0.94g/cm3
- LogP:2.40500
trans-4-MethoxycyclohexanaMine HCl (Cas 61367-41-7) Usage
Uses |
trans-4-Methylcyclohexylamine is used to characterize spermidine synthase of malaria parasite. |
Consumer Uses |
Buy trans-4-Methyl-cyclohexylamine hydrochloride (CAS 33483-65-7), a product for proteomics research, from Golden Pharma Co., Limited. |
61367-41-7 Relevant articles
Compounds and methods of use
-
Page/Page column 495; 496, (2021/08/04)
Compounds are provided according to Form...
Fragment-based Scaffold Hopping: Identification of Potent, Selective, and Highly Soluble Bromo and Extra Terminal Domain (BET) Second Bromodomain (BD2) Inhibitors
Seal, Jonathan T.,Atkinson, Stephen J.,Bamborough, Paul,Bassil, Anna,Chung, Chun-Wa,Foley, James,Gordon, Laurie,Grandi, Paola,Gray, James R. J.,Harrison, Lee A.,Kruger, Ryan G.,Matteo, Jeanne J.,McCabe, Michael T.,Messenger, Cassie,Mitchell, Darren,Phillipou, Alex,Preston, Alex,Prinjha, Rab K.,Rianjongdee, Francesco,Rioja, Inmaculada,Taylor, Simon,Wall, Ian D.,Watson, Robert J.,Woolven, James M.,Wyce, Anastasia,Zhang, Xi-Ping,Demont, Emmanuel H.
, p. 10772 - 10805 (2021/07/31)
The profound efficacy of pan-BET inhibit...
BENZIMIDAZOLYL-METHYL UREA DERIVATIVES AS ALX RECEPTOR AGONISTS
-
Page/Page column 106, (2015/02/25)
The present invention relates to benzimi...
TRI-SUBSTITUTED PYRIMIDINE COMPOUNDS AND THEIR USE AS PDE10 INHIBITORS
-
Page/Page column 28, (2011/07/08)
The present invention provides a tri-sub...
61367-41-7 Process route
- 56239-26-0
(1s,4s)-4-aminocyclohexan-1-ol hydrochloride
- 61367-41-7,5460-27-5
(1r,4r)-4-methoxycyclohexan-1-amine hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps
1: triethylamine / dichloromethane / 16 h / 21 °C
2: hydrogenchloride / 1,4-dioxane / 18 h / 21 °C
With hydrogenchloride; triethylamine; In 1,4-dioxane; dichloromethane;
|
- 760958-17-6
tert-butyl ((1r,4r)-4-methoxycyclohexyl)carbamate
- 61367-41-7,5460-27-5
(1r,4r)-4-methoxycyclohexan-1-amine hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride; In 1,4-dioxane; at 0 ℃; for 20h;
|
91% |
With hydrogenchloride; In 1,4-dioxane; at 21 ℃; for 18h;
|
84.56% |
With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 72h;
|
76% |
With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 1h;
|
|
With hydrogenchloride; In 1,4-dioxane; dichloromethane; at 0 ℃; for 2.5h; Inert atmosphere;
|
61367-41-7 Upstream products
-
760958-17-6
tert-butyl ((1r,4r)-4-methoxycyclohexyl)carbamate
-
111300-06-2
trans-tert-butyl 4-hydroxycyclohexylcarbamate
-
167081-25-6
cis-(4-hydroxycyclohexyl)carbamic acid tert-butyl ester
-
56239-26-0
(1s,4s)-4-aminocyclohexan-1-ol hydrochloride
61367-41-7 Downstream products
-
1214254-88-2
diethyl {[4-(trans-4-methoxycyclohexylamino)-6-pyrrolidin-1-ylpyrimidin-2-yl]methyl}phosphonate
-
1214254-89-3
2-[(E)-2-(6,7-difluoro-3-methylquinoxalin-2-yl)vinyl]-N-(trans-4-methoxycyclohexyl)-6-pyrrolidin-1-ylpyrimidin-4-amine
-
1214254-87-1
diethyl {[4-chloro-6-(trans-4-methoxycyclohexylamino)pyrimidin-2-yl]methyl}phosphonate
-
2222941-37-7
(S)-6-(5-(3,5-dimethylisoxazol-4-yl)-1-((1r,4S)-4-methoxycyclohexyl)-1H-benzo[d]imidazol-2-yl)-1-(3,4-difluorophenyl)piperidin-2-one
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