6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline

• CAS: 164148-92-9
• Catalog Number: ACM164148929
• Category: Other Products
• Molecular Weight: 248.32
• Molecular Formula: C₁₄H₂₀N₂O₂
• Synonyms: 6-AMINO-2-BOC-3,4-DIHYDRO-1H-ISOQUINOLINE;6-AMINO-2-N-BOC-1,2,3,4-TETRAHYDRO-ISOQUINOLINE;6-AMINO-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER;TERT-BUTYL 6-AMINO-3,4-DIHYDROISOQUINOLINE-2(1H)-CARBOXYLATE;2-Boc-6-amino-1,2,3,4-tetrahydroisoquinoline;REF DUPL: 6-Amino-2-N-Boc-1,2,3,4-tetrahydro-isoquinoline;2(1H)-Isoquinolinecarboxylic acid, 6-amino-3,4-dihydro-, 1,1-dimethylethyl ester;tert-butyl6-amino-1,4,4a,8a-tetrahydroisoquinoline-2(3H)-carboxylate
• Hazard Statements: Xn,N
• Safety Description: 26-36/37/39-61

Custom Q&A

What is the molecular formula of 6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline?

The molecular formula is C14H20N2O2.

What are the synonyms of 6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline?

Some synonyms include tert-butyl 6-amino-3,4-dihydro-1H-isoquinoline-2-carboxylate and 6-amino-2-n-boc-1,2,3,4-tetrahydro-isoquinoline.

What is the molecular weight of 6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline?

The molecular weight is 248.32 g/mol.

When was the 6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline created in PubChem?

It was created on 2005-07-19.

What is the IUPAC name of 6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline?

The IUPAC name is tert-butyl 6-amino-3,4-dihydro-1H-isoquinoline-2-carboxylate.

What is the InChIKey of 6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline?

The InChIKey is OLOIFCYZWOTWRO-UHFFFAOYSA-N.

How many hydrogen bond donor counts does 6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline have?

It has 1 hydrogen bond donor count.

What is the topological polar surface area of 6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline?

The topological polar surface area is 55.6Ų.

Does 6-Amino-2-N-boc-1,2,3,4-tetrahydro-isoquinoline have any defined atom stereocenter count?

No, it does not have any defined atom stereocenter count.

Is the compound canonicalized?

Yes, the compound is canonicalized.

Synthetic Use

Upstream Synthesis Route 1

• 1154424-63-1

• 164148-92-9

Reference: [1] Patent: WO2009/158571, 2009, A1, . Location in patent: Page/Page column 165; 167; 168

Upstream Synthesis Route 2

• 24424-99-5
• 72299-67-3

• 164148-92-9

Reference: [1] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 5, p. 2513 - 2528
[2] Patent: WO2007/11290, 2007, A1, . Location in patent: Page/Page column 13-15

Upstream Synthesis Route 3

• 170097-67-3

• 164148-92-9

Reference: [1] Patent: WO2009/158571, 2009, A1,

Downstream Synthesis Route 1

• 164148-92-9
• 30529-70-5

• 689165-95-5

Reference: [1]Patent: WO2004/39795,2004,A2 .Location in patent: Page 208-209

* For details of the synthesis route, please refer to the original source to ensure accuracy.