B73104

1-Bromonaphthalene

97%

Manufacturer: Sigma Aldrich

CAS Number: 90-11-9

Synonym(S): 1-Naphthyl bromide

Select a Size

Pack Size SKU Availability Price
5 G B73104-5-G In Stock ₹ 1,861.90
100 G B73104-100-G In Stock ₹ 2,533.05
500 G B73104-500-G In Stock ₹ 11,258.00

B73104 - 5 G

₹ 1,861.90

In Stock

Quantity

1

Base Price: ₹ 1,861.90

GST (18%): ₹ 335.142

Total Price: ₹ 2,197.042

Quality Level

200

Assay

97%

form

liquid

refractive index

n20/D 1.6570 (lit.)

bp

133-134 °C/10 mmHg (lit.)

mp

−2-−1 °C (lit.)

density

1.48 g/mL at 20 °C (lit.)

SMILES string

Brc1cccc2ccccc12

InChI

1S/C10H7Br/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H

InChI key

DLKQHBOKULLWDQ-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
501847895
Sigma Aldrich Fine Chemicals Biosciences 1-Bromonaphthalene 97% | 90-11-9 | MFCD00003868 | 100G
Sigma Aldrich Fine Chemicals Biosciences ₹ 8,437.07
501847896
Sigma Aldrich Fine Chemicals Biosciences 1-Bromonaphthalene 97% | 90-11-9 | MFCD00003868 | 500G
Sigma Aldrich Fine Chemicals Biosciences ₹ 16,246.13
501847894
Sigma Aldrich Fine Chemicals Biosciences 1-Bromonaphthalene >=95% | 90-11-9 | MFCD00003868 | 500ML
Sigma Aldrich Fine Chemicals Biosciences ₹ 40,037.80
NC2310691
eMolecules​ 1-Bromonaphthalene | 90-11-9 | MFCD00003868 | 10g
eMolecules​ ₹ 1,978.15
501847897
Sigma Aldrich Fine Chemicals Biosciences 1-Bromonaphthalene 97% | 90-11-9 | MFCD00003868 | 5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 6,049.09
17640
1-Bromonaphthalene
Sigma Aldrich ₹ 5,834.68 - ₹ 18,662.30
AR0033F8
1-Bromonaphthalene
Aaron Chemicals LLC ₹ 256.68 - ₹ 1,197.84
CS-0017140
1-Bromonaphthalene
ChemScene ₹ 513.36 - ₹ 4,791.36
AB43304
90-11-9 | 1-Bromonaphthalene
A2B Chem ₹ 427.80 - ₹ 3,422.40

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Description

  • General description: 1-Bromonaphthalene serves as an intermediate for the synthesis of biaryl compounds via cross-coupling reactions.[1][2]
  • Application: 1-Bromonaphthalene is a bromoarene that can be used in:Palladium-catalyzed Suzuki–Miyaura coupling reaction with potassium aryltrifluoroborates without the use of phase-transfer catalysts or phosphine ligands.[1]The preparation of indeno annelated polycyclic aromatic hydrocarbons by reacting with o-bromobenzeneboronic acid and oligocyclic bromoarenes via Suzuki-Heck type coupling.[3]Ni catalyzed Kumada–Tamao–Corriu cross-coupling reaction with PhMgBr.[2]The preparation of arylnaphthalenes via palladium-catalyzed Suzuki-Miyaura cross-coupling reaction with aryl boronic acid.[4]

SAFETY INFORMATION

Pictograms

GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H319,H410

Precautionary Statements

P264 - P270 - P273 - P280 - P301 + P312 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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form:
liquid

refractive index:
n20/D 1.6570 (lit.)

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133-134 °C/10 mmHg (lit.)

mp:
−2-−1 °C (lit.)

density:
1.48 g/mL at 20 °C (lit.)

SMILES string:
Brc1cccc2ccccc12

InChI:
1S/C10H7Br/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H

InChI key:
DLKQHBOKULLWDQ-UHFFFAOYSA-N

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Oc1ccc2ccccc2c1Br

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1S/C10H7BrO/c11-10-8-4-2-1-3-7(8)5-6-9(10)12/h1-6,12H

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FQJZPYXGPYJJIH-UHFFFAOYSA-N

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YLDFTMJPQJXGSS-UHFFFAOYSA-N

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