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N-(3-cyanophenyl)benzamide

Product Name
N-(3-cyanophenyl)benzamide
CAS No.
141990-91-2
Chemical Name
N-(3-cyanophenyl)benzamide
Synonyms
N-(3-Cyanophenyl);N-(3-cyanophenyl)benzamide;Benzamide, N-(3-cyanophenyl)-
CBNumber
CB61813942
Molecular Formula
C14H10N2O
Formula Weight
222.24
MOL File
141990-91-2.mol
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N-(3-cyanophenyl)benzamide Property

storage temp. 
Sealed in dry,Room Temperature
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
C955915
Product name
N-(3-Cyanophenyl)benzamide
Packaging
25mg
Price
$45
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC143783
Product name
N-(3-Cyanophenyl)benzamide
Packaging
250mg
Price
$70
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC143783
Product name
N-(3-Cyanophenyl)benzamide
Packaging
500mg
Price
$125
Updated
2021/12/16
Matrix Scientific
Product number
075386
Product name
N-(3-Cyanophenyl)benzamide
Purity
95+%
Packaging
250mg
Price
$260
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC143783
Product name
N-(3-Cyanophenyl)benzamide
Packaging
2g
Price
$372
Updated
2021/12/16
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N-(3-cyanophenyl)benzamide Chemical Properties,Usage,Production

Synthesis

93-58-3

2237-30-1

141990-91-2

GENERAL PROCEDURE: Pure m-aminobenzonitrile (1.00 mmol) and methyl benzoate (1.00 mmol) with DABAL-Me3 (202 mg, 0.8 eq.) are placed in a 5 mL microwaveable vial and dry tetrahydrofuran (1 mL) is added under argon protection. For coupled spouses containing acidic hydrogen, additional DABAL-Me3 (410 mg, 1.6 eq. total) is added. The vials were quickly capped and placed in a CEM Discover microwave reactor. Irradiation was carried out at 130 °C for 8 min at 290 W power, followed by programmed cooling (~20 min). The reaction was quenched by careful addition of 2 M hydrochloric acid (4 mL) or saturated potassium sodium tartrate solution (4 mL) (note: methane may be released). The reaction mixture is extracted with dichloromethane, dried over magnesium sulfate and concentrated to give pure N-(3-cyanophenyl)benzamide directly. For further purification, the amides lacking highly polar functional groups can be separated by column chromatography using 3:2 to 2:3 hexane:ethyl acetate as eluent; for amides containing polar functional groups such as side-chain amines, alcohols, etc., dichloromethane containing 2% v/v methanol is used as eluent.

References

[1] Tetrahedron, 2013, vol. 69, # 46, p. 9890 - 9897

N-(3-cyanophenyl)benzamide Preparation Products And Raw materials

Raw materials

Preparation Products

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N-(3-cyanophenyl)benzamide Suppliers

SynAsst Chemical.
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021-60343070
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China
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Shanghai Jovan Biochemical Technology Co. Ltd.
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+86-021-61654350
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+86-021-61654350
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China
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DebyeTec.com Inc.
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18086626237 18086626237
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qq:2693528373
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Chengdu Research Accelerators Technology Co., Ltd.
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028-64353063 QQ:784253935
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Zhengzhou kangnuochenrui Chemical Technology Co.,Ltd
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Amadis Chemical Company Limited
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Yantai ShengKailun Chemical Technology Co., Ltd.
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Hangzhou Molcore Biopharmatech Co.,Ltd
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Aikon International Limited
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141990-91-2, N-(3-cyanophenyl)benzamideRelated Search:


  • N-(3-cyanophenyl)benzamide
  • N-(3-Cyanophenyl)
  • Benzamide, N-(3-cyanophenyl)-
  • 141990-91-2