6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

• CAS: 2328-12-3
• Catalog Number: ACM2328123
• Category: Other Products
• Molecular Weight: 229.7
• Molecular Formula: C₁₁H₁₆ClNO₂
• Synonyms: TIMTEC-BB SBB003285;1,2,3,4-tetrahydro-6,7-dimethoxy-isoquinolinhydrochloride;1,2,3,4-TETRAHYDRO-6,7-DIMETHOXY-ISOQUINOLINE HYDROCHLORIDE;6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE HYDROCHLORIDE;LABOTEST-BB LT00453025;ISOQUINOLINE, 1,2,3,4-TETRAHYDRO-6,7-DIMETHOXY-, HYDROCHLORIDE;6,7-Dimethoxy-1,2,3,4-tetrahyroisoquinoline hydrochloride, 97%;6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinolineHCl
• Melting Point: 260-265°C(lit.)
• Hazard Statements: Xi
• Safety Description: 26-36
• Supplemental Hazard Statements: H315-H319-H335
• Symbol: GHS07

Custom Q&A

What is the molecular formula of 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

The molecular formula of 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride is C11H16ClNO2.

What is the molecular weight of 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

The molecular weight of 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride is 229.70 g/mol.

What are some synonyms for 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

Some synonyms for 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride include 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline, and MFCD00012744.

What is the InChIKey for 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

The InChIKey for 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride is SHOWAGCIRTUYNA-UHFFFAOYSA-N.

What is the Canonical SMILES representation of 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

The Canonical SMILES representation of 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride is COC1=C(C=C2CNCCC2=C1)OC.Cl.

What is the CAS number for 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

The CAS number for 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride is 2328-12-3.

How many hydrogen bond donor counts does 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride have?

6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride has 2 hydrogen bond donor counts.

What is the exact mass of 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

The exact mass of 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride is 229.0869564 g/mol.

How many heavy atoms does 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride contain?

6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride contains 15 heavy atoms.

Does 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride have any defined or undefined bond stereocenters?

No, 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride does not have any defined or undefined bond stereocenters.

Synthetic Use

Upstream Synthesis Route 1

• 50-00-0
• 120-20-7

• 2328-12-3

Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 20, p. 5285 - 5289
[2] Patent: CN107573325, 2018, A, . Location in patent: Paragraph 0109; 0110; 0111
[3] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 9, p. 2420 - 2427
[4] Pharmazie, 1990, vol. 45, # 6, p. 408 - 410
[5] Journal of the American Chemical Society, 1934, vol. 56, p. 1769

Upstream Synthesis Route 2

• 26259-07-4

• 2328-12-3

Reference: [1] Patent: US2008/33177, 2008, A1, . Location in patent: Page/Page column 10-11

Upstream Synthesis Route 3

• 109-87-5
• 120-20-7

• 2328-12-3

Reference: [1] European Journal of Medicinal Chemistry, 1981, vol. 16, # 6, p. 508 - 514

Upstream Synthesis Route 4

• 50-00-0
• 120-20-7

• 2328-12-3

Reference: [1]Zhu, Ju; Lu, Jiaguo; Zhou, Youjun; Li, Yaowu; Cheng, Jun; Zheng, Canhui
[Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 20, p. 5285 - 5289]

Downstream Synthesis Route 1

• 2274-11-5
• 2328-12-3

• 81165-87-9

Reference: [1]Stenlake; Waigh; Urwin; et al.
[European Journal of Medicinal Chemistry, 1981, vol. 16, # 6, p. 508 - 514]

Downstream Synthesis Route 2

• 2328-12-3

• 52768-23-7

Reference: [1]Orjales, Aurelio; Mosquera, Ramón; Toledo, Antonio; Pumar, M. Carmen; García, Neftalí; Cortizo, Lourdes; Labeaga, Luis; Innerárity, Ana
[Journal of Medicinal Chemistry, 2003, vol. 46, # 25, p. 5512 - 5532]

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