Ethyl (6-amino-2,3-dichlorobenzyl)glycinate hydrochloride

95%

Reagent Code: #180817
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CAS Number 85325-12-8

science Other reagents with same CAS 85325-12-8

blur_circular Chemical Specifications

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Weight 313.61 g/mol
Formula C₁₁H₁₅Cl₃N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of antihypertensive drugs like valsartan and related sartan-class medications. Its structure allows for the construction of the core benzyl amino acid framework essential for biological activity in these pharmaceuticals. Commonly employed in multi-step organic synthesis due to its protected amine group and reactive ester functionality, enabling peptide-like coupling and subsequent cyclization reactions. Widely utilized in the pharmaceutical industry for large-scale manufacturing of cardiovascular drugs.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿19,260.00

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Ethyl (6-amino-2,3-dichlorobenzyl)glycinate hydrochloride
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Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of antihypertensive drugs like valsartan and related sartan-class medications. Its structure allows for the construction of the core benzyl amino acid framework essential for biological activity in these pharmaceuticals. Commonly employed in multi-step organic synthesis due to its protected amine group and reactive ester functionality, enabling peptide-like coupling and subsequent cyclizatio

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of antihypertensive drugs like valsartan and related sartan-class medications. Its structure allows for the construction of the core benzyl amino acid framework essential for biological activity in these pharmaceuticals. Commonly employed in multi-step organic synthesis due to its protected amine group and reactive ester functionality, enabling peptide-like coupling and subsequent cyclization reactions. Widely utilized in the pharmaceutical industry for large-scale manufacturing of cardiovascular drugs.

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