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2412-58-0,MFCD00047648
Catalog No.:AA00BIZL

2412-58-0 | 1-Methyl-3,4-dihydroisoquinoline

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$60.00   $42.00
- +
1g
95%
in stock  
$84.00   $59.00
- +
5g
95%
in stock  
$358.00   $251.00
- +
25g
95%
in stock  
$1,316.00 $922.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00BIZL
Chemical Name:
1-Methyl-3,4-dihydroisoquinoline
CAS Number:
2412-58-0
Molecular Formula:
C10H11N
Molecular Weight:
145.2010
MDL Number:
MFCD00047648
SMILES:
CC1=NCCc2c1cccc2
NSC Number:
27893
Properties
Computed Properties
 
Complexity:
172  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.6  

Literature

Title: Novel 5, 6-Dihydropyrrolo[2,1-a]isoquinolines as Scaffolds for Synthesis of Lamellarin Analogues.

Journal: Evidence-based complementary and alternative medicine : eCAM 20110101

Title: Effects of a structural analogue of salsolinol, 1-MeDIQ, on pituitary prolactin release and dopaminergic activity in the mediobasal hypothalamus in nursing sheep.

Journal: Brain research 20100111

Title: Effects of salsolinol and its antagonistic analogue, 1-MeDIQ, on growth hormone release in nursing sheep.

Journal: Acta neurobiologiae experimentalis 20100101

Title: The role of catecholamines in the prolactin release induced by salsolinol.

Journal: Neurochemistry international 20071001

Title: The peripheral noradrenergic terminal as possible site of action of salsolinol as prolactoliberin.

Journal: Neurochemistry international 20070101

Title: Identification of the endogenous key substrates of the human organic cation transporter OCT2 and their implication in function of dopaminergic neurons.

Journal: PloS one 20070101

Title: Formalin attenuates the stress-induced increase in plasma epinephrine levels.

Journal: Journal of neuroendocrinology 20051101

Title: Salsolinol, an antagonist of prolactoliberine, induces an increase in plasma catecholamine levels in the rat.

Journal: Autonomic neuroscience : basic & clinical 20040930

Title: Pivotal role of an endogenous tetrahydroisoquinoline, salsolinol, in stress- and suckling-induced release of prolactin.

Journal: Annals of the New York Academy of Sciences 20040601

Title: Stress- as well as suckling-induced prolactin release is blocked by a structural analogue of the putative hypophysiotrophic prolactin-releasing factor, salsolinol.

Journal: Journal of neuroendocrinology 20040301

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SDS
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Tags:2412-58-0 Molecular Formula|2412-58-0 MDL|2412-58-0 SMILES|2412-58-0 1-Methyl-3,4-dihydroisoquinoline
Catalog No.: AA00BIZL
2412-58-0,MFCD00047648
2412-58-0 | 1-Methyl-3,4-dihydroisoquinoline
Pack Size： 250mg
Purity： 95%
in stock
$60.00 $42.00
Pack Size： 1g
Purity： 95%
in stock
$84.00 $59.00
Pack Size： 5g
Purity： 95%
in stock
$358.00 $251.00
Pack Size： 25g
Purity： 95%
in stock
$1,316.00 $922.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00BIZL
Chemical Name: 1-Methyl-3,4-dihydroisoquinoline
CAS Number: 2412-58-0
Molecular Formula: C10H11N
Molecular Weight: 145.2010
MDL Number: MFCD00047648
SMILES: CC1=NCCc2c1cccc2
NSC Number: 27893
Properties
Complexity: 172  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.6  
Literature fold

Title: Novel 5, 6-Dihydropyrrolo[2,1-a]isoquinolines as Scaffolds for Synthesis of Lamellarin Analogues.

Journal: Evidence-based complementary and alternative medicine : eCAM20110101

Title: Effects of a structural analogue of salsolinol, 1-MeDIQ, on pituitary prolactin release and dopaminergic activity in the mediobasal hypothalamus in nursing sheep.

Journal: Brain research20100111

Title: Effects of salsolinol and its antagonistic analogue, 1-MeDIQ, on growth hormone release in nursing sheep.

Journal: Acta neurobiologiae experimentalis20100101

Title: The role of catecholamines in the prolactin release induced by salsolinol.

Journal: Neurochemistry international20071001

Title: The peripheral noradrenergic terminal as possible site of action of salsolinol as prolactoliberin.

Journal: Neurochemistry international20070101

Title: Identification of the endogenous key substrates of the human organic cation transporter OCT2 and their implication in function of dopaminergic neurons.

Journal: PloS one20070101

Title: Formalin attenuates the stress-induced increase in plasma epinephrine levels.

Journal: Journal of neuroendocrinology20051101

Title: Salsolinol, an antagonist of prolactoliberine, induces an increase in plasma catecholamine levels in the rat.

Journal: Autonomic neuroscience : basic & clinical20040930

Title: Pivotal role of an endogenous tetrahydroisoquinoline, salsolinol, in stress- and suckling-induced release of prolactin.

Journal: Annals of the New York Academy of Sciences20040601

Title: Stress- as well as suckling-induced prolactin release is blocked by a structural analogue of the putative hypophysiotrophic prolactin-releasing factor, salsolinol.

Journal: Journal of neuroendocrinology20040301

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