(S)-(-)-3-tert-Butylamino-1,2-propanediol

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Reagent Code: #234614
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CAS Number 30315-46-9

science Other reagents with same CAS 30315-46-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.22 g/mol
Formula (CH₃)₃CNHCH₂CH(OH)CH₂OH
badge Registry Numbers
EC Number 250-125-1
MDL Number MFCD00190165
thermostat Physical Properties
Melting Point 85-89 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of beta-blocker pharmaceuticals, particularly in the production of (S)-propranolol and other cardioselective agents. Its stereochemistry enables high enantioselectivity in drug synthesis, improving therapeutic efficacy and reducing side effects. Also employed in asymmetric synthesis for developing adrenergic receptor modulators. Commonly utilized in research settings for catalyzing enantioselective transformations and in the preparation of optically active amines.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿162.00
5g
10-20 days ฿203.50
25g
10-20 days ฿906.00
100g
10-20 days ฿5,110.00
500g
10-20 days ฿12,402.00

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(S)-(-)-3-tert-Butylamino-1,2-propanediol
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Used as a key chiral intermediate in the synthesis of beta-blocker pharmaceuticals, particularly in the production of (S)-propranolol and other cardioselective agents. Its stereochemistry enables high enantioselectivity in drug synthesis, improving therapeutic efficacy and reducing side effects. Also employed in asymmetric synthesis for developing adrenergic receptor modulators. Commonly utilized in research settings for catalyzing enantioselective transformations and in the preparation of optically acti

Used as a key chiral intermediate in the synthesis of beta-blocker pharmaceuticals, particularly in the production of (S)-propranolol and other cardioselective agents. Its stereochemistry enables high enantioselectivity in drug synthesis, improving therapeutic efficacy and reducing side effects. Also employed in asymmetric synthesis for developing adrenergic receptor modulators. Commonly utilized in research settings for catalyzing enantioselective transformations and in the preparation of optically active amines.

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