Home Cart Sign in  
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 613-90-1 Chemical Structure| 613-90-1
Chemical Structure| 613-90-1

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Synonyms: Benzoyl Cyanide

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Benzoyl Cyanide

CAS No. :613-90-1
Formula : C8H5NO
M.W : 131.13
SMILES Code : O=C(C#N)C1=CC=CC=C1
Synonyms :
Benzoyl Cyanide
MDL No. :MFCD00001837
InChI Key :GJQBHOAJJGIPRH-UHFFFAOYSA-N
Pubchem ID :11953

Safety of Benzoyl Cyanide

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H300-H311+H331-H315-H319-H400
Precautionary Statements:P501-P261-P273-P270-P271-P264-P280-P391-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405
Class:6.1
UN#:3439
Packing Group:

Application In Synthesis of Benzoyl Cyanide

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 613-90-1 ]

[ 613-90-1 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 613-90-1 ]
  • [ 50607-30-2 ]
  • 3-benzoylpiperidine-2,4-dione [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine;Zinc chloride; In dichloromethane; EXAMPLE 12 Compound 66 Dry triethylamine (1.33 g) was added at 0°-5° C. to a stirred suspension of <strong>[50607-30-2]piperidine-2,4-dione</strong> (1.13 g), anhydrous zinc chloride (1.64 g) and benzoyl cyanide (1.31 g) in dry dichloromethane (50 ml) and the mixture stirred at ambient temperature for 18 hours. The mixture was washed successively with 2N hydrochloric acid (2*30 ml) and water (3*30 ml) dried over magnesium sulphate and evaporated under reduced pressure to give a pale yellow solid which was recrystallized from acetonitrile (0.5 ml) to give 3-benzoyl<strong>[50607-30-2]piperidine-2,4-dione</strong> (0.5 g), mp 164°-165° C., as a cream crystalline solid.
  • 2
  • [ 126-33-0 ]
  • [ 98-88-4 ]
  • [ 613-90-1 ]
YieldReaction ConditionsOperation in experiment
With sodium benzoate; EXAMPLE 9 72 g (0.5 mol) of sodium benzoate were mixed with 140.6 g (1 mol) of benzoyl chloride and 80 ml of tetramethylene-sulphone and 25 g (0.5 mol) of 98% pure sodium cyanide. After a stirring time of 20 minutes, an exothermic rise in the temperature to 85 C. was observed. It was now easier to stir the mixture. The subsequent reaction time was 2.5 hours at 150-160 C. Working up gave the following yield: 65 g (99.3% of theory) of benzoyl cyanide; melting point 34 C.
  • 3
  • [ 613-90-1 ]
  • [ 41394-05-2 ]
  • 4
  • [ 613-90-1 ]
  • [ 48149-72-0 ]
  • allyl 2,4,6-tri-O-benzoyl-α-D-galactopyranoside [ No CAS ]
  • 5
  • [ 613-90-1 ]
  • [ 667463-64-1 ]
  • 6-bromo-3-cyano-1-methyl-2-oxoindolin-3-yl benzoate [ No CAS ]
  • 6
  • [ 613-90-1 ]
  • [ 20651-67-6 ]
  • [ 75-20-7 ]
  • (Z)-2-(4-butylphenyl)-4-oxo-4-phenylbut-2-enenitrile [ No CAS ]
  • 7
  • [ 613-90-1 ]
  • [ 626-01-7 ]
  • [ 141990-91-2 ]
  • 8
  • [ 613-90-1 ]
  • [ 660-49-1 ]
  • N-(3-cyano-5-fluorophenyl)benzamide [ No CAS ]
  • 9
  • [ 613-90-1 ]
  • [ 552331-00-7 ]
  • N-(4-cyanopyridin-2-yl)benzamide [ No CAS ]
  • 10
  • [ 613-90-1 ]
  • [ 6563-13-9 ]
  • [ 19062-82-9 ]
YieldReaction ConditionsOperation in experiment
78% With graphene oxide; In dimethyl sulfoxide; at 100℃; for 8h; General procedure: A 2-dram vial equipped with a magnetic stir bar was charged with quinoline N-oxide (0.3 mmol, 44 mg), benzoyl cyanide (1.5 equiv, 59 mg), GO (50 wt %, 22 mg), and DMSO (1 mL) under an air atmosphere. The reaction mixture was placed in an oil bath and stirred at 100 oC for 8 h. The reaction mixture was cooled down to room temperature and diluted with H2O (15 mL). The reaction mixture was then extracted with ethyl acetate (3 X 5 mL) and the combined organic layers were dried over Na2SO4. The solution was concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (eluent: EtOAc/PE = 1:2) to yield the corresponding product 2.
 

Historical Records

Technical Information

Categories