Catalog No.:AA003NDZ

6960-42-5 | 7-Nitroindole

Name: Name:7-Nitroindole
Brand: AABLOCKS
SKU: AA003NDZ
Availability: InStock
Rating: 90 (10 reviews)

Pack Size

Purity

Availability

Price(USD)

Quantity

98%

in stock

$6.00 $4.00

- +

98%

in stock

$16.00 $11.00

- +

10g

98%

in stock

$28.00 $20.00

- +

25g

98%

in stock

$70.00 $49.00

- +

100g

98%

in stock

$253.00 $178.00

- +

Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
Download SDS

Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003NDZ

Chemical Name:

7-Nitroindole

CAS Number:

6960-42-5

Molecular Formula:

C8H6N2O2

Molecular Weight:

162.1454

MDL Number:

MFCD00005683

SMILES:

[O-][N+](=O)c1cccc2c1[nH]cc2

NSC Number:

69874

Properties

BP:

362.6 °C at 760 mmHg

Form:

Solid

MP:

94-98 °C(lit.)

Refractive Index:

1.5770 (estimate)

Storage:

Room Temperature;

Computed Properties

Complexity:

190

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

XLogP3:

2.6

Upstream Synthesis Route

6960-45-8

6960-42-5

[1]Patent:EP2366687,2011,A2,.Locationinpatent:Page/Pagecolumn8;10-11

[2]JournaloftheAmericanChemicalSociety,1958,vol.80,p.4621

[3]JournalofOrganicChemistry,1957,vol.22,p.84

[4]JournalandProceedingsoftheRoyalSocietyofNewSouthWales,1938,vol.72,p.209,216

[5]JournaloftheAmericanChemicalSociety,1958,vol.80,p.4621

[6]JournalofOrganicChemistry,1957,vol.22,p.84

[7]JournalofAgriculturalandFoodChemistry,2016,vol.64,#24,p.4830-4837

53924-05-3

6960-42-5

[1]JournaloftheAmericanChemicalSociety,2009,vol.131,#36,p.12898-12899

1826-67-1

528-29-0

6960-42-5

[1]Tetrahedron,2008,vol.64,#3,p.568-574

[2]OrganicLetters,2013,vol.15,#18,p.4730-4733

6960-46-9

6960-42-5

[1]JournaloftheAmericanChemicalSociety,1958,vol.80,p.4621

[2]JournalofOrganicChemistry,1957,vol.22,p.84

[3]Patent:EP2366687,2011,A2,

[4]JournalofAgriculturalandFoodChemistry,2016,vol.64,#24,p.4830-4837

292853-66-8

6960-42-5

[1]JournaloftheAmericanChemicalSociety,1958,vol.80,p.4621

[2]JournalofOrganicChemistry,1957,vol.22,p.84

[3]Patent:EP2366687,2011,A2,

Downstream Synthesis Route

6960-45-8

6960-42-5

[1]Patent:EP2366687,2011,A2.Locationinpatent:Page/Pagecolumn8;10-11

[2]JournaloftheAmericanChemicalSociety,1958,vol.80,p.4621

[3]JournalandProceedings-RoyalSocietyofNewSouthWales,1938,vol.72,p.209,216

[4]JournaloftheAmericanChemicalSociety,1958,vol.80,p.4621

[5]JournalofAgriculturalandFoodChemistry,2016,vol.64,p.4830-4837

6960-42-5

5192-04-1

[1]Patent:WO2004/67529,2004,A1.Locationinpatent:Page75-76

[2]Patent:WO2005/92854,2005,A1.Locationinpatent:Page/Pagecolumn53

[3]GreenChemistry,2017,vol.19,p.809-815

[4]SyntheticCommunications,2018,vol.48,p.2475-2484

[5]Patent:WO2005/92854,2005,A1.Locationinpatent:Page/Pagecolumn56-57

[6]TetrahedronLetters,2019,vol.60,p.948-952

[7]TetrahedronLetters,1995,vol.36,p.2411-2414

[8]EuropeanJournalofOrganicChemistry,2009,p.4854-4866

[9]Tetrahedron,2008,vol.64,p.568-574

[10]OrganicandBiomolecularChemistry,2014,vol.13,p.925-937

[11]JournalofMedicinalChemistry,1995,vol.38,p.1942-1954

[12]JournalofMedicinalChemistry,1999,vol.42,p.3789-3799

[13]JournalofMedicinalChemistry,2002,vol.45,p.4913-4922

[14]JournalofMedicinalChemistry,2007,vol.50,p.6443-6445

[15]Patent:US2004/63733,2004,A1

[16]ChemicalCommunications,2009,p.6279-6281

[17]Patent:EP2366687,2011,A2.Locationinpatent:Page/Pagecolumn24-25

[18]OrganicandBiomolecularChemistry,2012,vol.10,p.5909-5915

[19]Patent:WO2012/115479,2012,A2.Locationinpatent:Page/Pagecolumn19-20

[20]OrganicLetters,2013,vol.15,p.4730-4733

[21]Synthesis,2015,vol.47,p.861-870

[22]JournalofAgriculturalandFoodChemistry,2016,vol.64,p.4830-4837

[23]EuropeanJournalofOrganicChemistry,2018,vol.2018,p.209-214

[24]RSCAdvances,2018,vol.8,p.8898-8909

[25]AppliedCatalysisA:General,2018,vol.559,p.127-137

[26]Patent:WO2019/197546,2019,A1.Locationinpatent:Page/Pagecolumn33;42

6960-42-5

4330-21-6

218167-11-4

[1]Chemistry-AEuropeanJournal,2000,vol.6,p.4163-4169

[2]JournaloftheAmericanChemicalSociety,1998,vol.120,p.11810-11811

6960-42-5

165669-14-7

[1]JournalofMedicinalChemistry,1999,vol.42,p.3789-3799

[2]Patent:US5721246,1998,A

6960-42-5

397864-11-8

[1]Patent:WO2018/33082,2018,A1.Locationinpatent:Paragraph00327

[2]Patent:WO2004/67529,2004,A1.Locationinpatent:Page76

[3]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.2535-2538

Literature

Title: Direct functionalization of (un)protected tetrahydroisoquinoline and isochroman under iron and copper catalysis: two metals, two mechanisms.

Journal: The Journal of organic chemistry 20111104

Title: A novel role of prostaglandin E2 in neuropathic pain: blockade of microglial migration in the spinal cord.

Journal: Glia 20110201

Title: Rapid S-nitrosylation of actin by NO-generating donors and in inflammatory pain model mice.

Journal: Molecular pain 20110101

Quotation Request

Company Name:

Contact Person:

Email:

Quantity Required:

Country:

Additional Info:

SDS