136581

1,5-Diazabicyclo[4.3.0]non-5-ene

98%

Manufacturer: Sigma Aldrich

CAS Number: 3001-72-7

Synonym(S): DBN

Select a Size

Pack Size SKU Availability Price
5 G 136581-5-G In Stock ₹ 1,898.10
25 G 136581-25-G In Stock ₹ 5,217.00
100 G 136581-100-G In Stock ₹ 16,261.50

136581 - 5 G

₹ 1,898.10

In Stock

Quantity

1

Base Price: ₹ 1,898.10

GST (18%): ₹ 341.658

Total Price: ₹ 2,239.758

Quality Level

200

Assay

98%

form

liquid

refractive index

n20/D 1.519 (lit.)

bp

95-98 °C/7.5 mmHg (lit.)

density

1.005 g/mL at 25 °C (lit.)

SMILES string

C1CN=C2CCCN2C1

InChI

1S/C7H12N2/c1-3-7-8-4-2-6-9(7)5-1/h1-6H2

InChI key

SGUVLZREKBPKCE-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
33471
1,5-Diazabicyclo[4.3.0]non-5-ene
Sigma Aldrich ₹ 7,459.20 - ₹ 87,112.80
136581
1,5-Diazabicyclo[4.3.0]non-5-ene
Sigma Aldrich ₹ 1,898.10 - ₹ 16,261.50
33471
1,5-Diazabicyclo[4.3.0]non-5-ene
Sigma Aldrich ₹ 7,459.20 - ₹ 87,112.80
CS-W016569
DBN
ChemScene ₹ 1,197.84 - ₹ 24,812.40
AB57550
3001-72-7 | 1,5-Diazabicyclo[4.3.0]non-5-ene
A2B Chem ₹ 427.80 - ₹ 13,518.48

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Description

  • General description: DBN is a strong base widely used as a catalyst in organic synthesis to facilitate Michael additions and aldol condensations.[1][2][3]
  • Application: 1,5-Diazabicyclo[4.3.0]non-5-ene (DBN) can be used as:        A reagent for the synthesis of β-carbolines from tetrahydro-β-carbolines via dehydrogenative/decarboxylative aromatization.[4]        A nucleophilic organocatalyst in the regioselective C-acylation of pyrroles and indoles by Friedel−Crafts acylation reaction.[1]  A superbase in the formulation of a ternary liquid-liquid phase changing system, along with hexadecane and hexanol, to capture hydrogen sulfide gas.[5]       A base for the preparation of 1H-quinazoline-2,4-diones from 2-aminobenzonitriles using supercritical carbon dioxide as a reactant and a solvent.[6]  A catalyst for the synthesis of benzothiazolones by the reaction between 2-aminothiophenols and CO2 by cyclocarbonylation reaction via C-S bond formation.[2]

SAFETY INFORMATION

Pictograms

GHS05

Signal Word

Danger

Hazard Statements

H314

Precautionary Statements

P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405

Hazard Classifications

Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

201.2 °F

Flash Point(C)

94 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Quality Level:
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Assay:
98%

form:
liquid

refractive index:
n20/D 1.519 (lit.)

bp:
95-98 °C/7.5 mmHg (lit.)

density:
1.005 g/mL at 25 °C (lit.)

SMILES string:
C1CN=C2CCCN2C1

InChI:
1S/C7H12N2/c1-3-7-8-4-2-6-9(7)5-1/h1-6H2

InChI key:
SGUVLZREKBPKCE-UHFFFAOYSA-N

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CCN(CC)CC(=O)Nc1c(C)cccc1C

InChI:
1S/C14H22N2O/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4/h7-9H,5-6,10H2,1-4H3,(H,15,17)

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NNJVILVZKWQKPM-UHFFFAOYSA-N

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SMILES string:
Cc1cccc(C)c1NC(=O)CCl

InChI:
1S/C10H12ClNO/c1-7-4-3-5-8(2)10(7)12-9(13)6-11/h3-5H,6H2,1-2H3,(H,12,13)

InChI key:
FPQQSNUTBWFFLB-UHFFFAOYSA-N

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SMILES string:
__

InChI:
__

InChI key:
__