2-amino-2-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)acetic acid hydrochloride

95%

Reagent Code: #196534
fingerprint
CAS Number 147900-41-2

science Other reagents with same CAS 147900-41-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.78 g/mol
Formula C₁₇H₁₈ClNO₂
badge Registry Numbers
MDL Number MFCD30471992
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily in pharmaceutical research as a key intermediate in the synthesis of tricyclic antidepressants, particularly analogs of amitriptyline and imipramine. Its structure supports the development of compounds with modulatory effects on neurotransmitter reuptake, especially serotonin and norepinephrine. Due to the presence of both amino and carboxylic acid functional groups, it serves as a versatile building block for creating bioactive molecules with enhanced blood-brain barrier penetration. Also employed in the preparation of labeled derivatives for metabolic and receptor binding studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿68,990.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-amino-2-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)acetic acid hydrochloride
No image available

Used primarily in pharmaceutical research as a key intermediate in the synthesis of tricyclic antidepressants, particularly analogs of amitriptyline and imipramine. Its structure supports the development of compounds with modulatory effects on neurotransmitter reuptake, especially serotonin and norepinephrine. Due to the presence of both amino and carboxylic acid functional groups, it serves as a versatile building block for creating bioactive molecules with enhanced blood-brain barrier penetration. Also

Used primarily in pharmaceutical research as a key intermediate in the synthesis of tricyclic antidepressants, particularly analogs of amitriptyline and imipramine. Its structure supports the development of compounds with modulatory effects on neurotransmitter reuptake, especially serotonin and norepinephrine. Due to the presence of both amino and carboxylic acid functional groups, it serves as a versatile building block for creating bioactive molecules with enhanced blood-brain barrier penetration. Also employed in the preparation of labeled derivatives for metabolic and receptor binding studies.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...