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Structure

6-Bromo-1,2,3,4-tetrahydroquinoline

CAS
22190-35-8
Catalog Number
ACM22190358
Category
Bromine Series
Molecular Weight
212.09
Molecular Formula
C9H10NBr

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What is the molecular formula of 6-Bromo-1,2,3,4-tetrahydroquinoline?

The molecular formula of 6-Bromo-1,2,3,4-tetrahydroquinoline is C9H10BrN.

When was 6-Bromo-1,2,3,4-tetrahydroquinoline created?

6-Bromo-1,2,3,4-tetrahydroquinoline was created on September 16, 2005.

What is the IUPAC Name of 6-Bromo-1,2,3,4-tetrahydroquinoline?

The IUPAC Name of 6-Bromo-1,2,3,4-tetrahydroquinoline is 6-bromo-1,2,3,4-tetrahydroquinoline.

What is the InChIKey for 6-Bromo-1,2,3,4-tetrahydroquinoline?

The InChIKey for 6-Bromo-1,2,3,4-tetrahydroquinoline is WEHMHBSITKCQBY-UHFFFAOYSA-N.

What is the molecular weight of 6-Bromo-1,2,3,4-tetrahydroquinoline?

The molecular weight of 6-Bromo-1,2,3,4-tetrahydroquinoline is 212.09 g/mol.

How many Hydrogen Bond Donor Counts does 6-Bromo-1,2,3,4-tetrahydroquinoline have?

6-Bromo-1,2,3,4-tetrahydroquinoline has 1 Hydrogen Bond Donor Count.

What is the Exact Mass of 6-Bromo-1,2,3,4-tetrahydroquinoline?

The Exact Mass of 6-Bromo-1,2,3,4-tetrahydroquinoline is 210.99966 g/mol.

What is the Rotatable Bond Count of 6-Bromo-1,2,3,4-tetrahydroquinoline?

The Rotatable Bond Count of 6-Bromo-1,2,3,4-tetrahydroquinoline is 0.

Is the Compound Is Canonicalized for 6-Bromo-1,2,3,4-tetrahydroquinoline?

Yes, the Compound Is Canonicalized for 6-Bromo-1,2,3,4-tetrahydroquinoline.

How many Heavy Atoms are present in 6-Bromo-1,2,3,4-tetrahydroquinoline?

There are 11 Heavy Atoms present in 6-Bromo-1,2,3,4-tetrahydroquinoline.

Upstream Synthesis Route 1

  • 5332-25-2
  • 22190-35-8

Reference: [1] Chemical Communications, 2013, vol. 49, # 63, p. 7052 - 7054

Upstream Synthesis Route 2

  • 635-46-1
  • 22190-35-8

Reference: [1] Tetrahedron, 2005, vol. 61, # 16, p. 4035 - 4041

Upstream Synthesis Route 3

  • 76228-06-3
  • 22190-35-8

Reference: [1]Bioorganic and Medicinal Chemistry Letters,2007,vol. 17,p. 6481 - 6488

Downstream Synthesis Route 1

  • 22190-35-8
  • 5332-25-2

Reference: [1] Organic Letters, 2015, vol. 17, # 18, p. 4404 - 4407

Downstream Synthesis Route 2

  • 22190-35-8
  • 125076-71-3

Reference: [1]Journal of Organic Chemistry,1990,vol. 55,p. 1744 - 1749

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

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