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60299-77-6

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60299-77-6 Usage

Synthesis Reference(s)

Tetrahedron Letters, 26, p. 925, 1985 DOI: 10.1016/S0040-4039(00)61966-4

Check Digit Verification of cas no

The CAS Registry Mumber 60299-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,9 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60299-77:
(7*6)+(6*0)+(5*2)+(4*9)+(3*9)+(2*7)+(1*7)=136
136 % 10 = 6
So 60299-77-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H7NO/c11-8-10(12)7-6-9-4-2-1-3-5-9/h1-7H/b7-6+

60299-77-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-phenylprop-2-enoyl cyanide

1.2 Other means of identification

Product number -
Other names Benzylidenbrenztraubensaeure-nitril

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60299-77-6 SDS

60299-77-6Relevant articles and documents

Spontaneous Dimerization of Allenes in Situ: An Efficient Synthesis of Substituted 1,2-Dimethylenecyclobutanes with High Regio- and Stereoselectivities

Miao, Maozhong,Wang, Wenmin,Yang, Weijun,Xu, Lijun,Ma, Jing,Ren, Hongjun

, p. 14447 - 14453 (2015)

An intermolecular [2+2] cycloaddition reaction for the synthesis of 1,2-dimethylenecyclobutane derivatives from the commercially available starting materials aryl acetylenes, nBuLi, formamides, and trimethylsilyl cyanide (TMSCN) has been achieved. This reaction displays high regio- and stereoselectivities due to the captodative effect. The mechanism of the reaction has been investigated by the deuterium labeling experiments and DFT calculations. Cycloaddition of captodative allenes: A regio- and stereoselective intermolecular [2+2] cycloaddition of captodative allenes (in situ generated) for the efficient synthesis of substituted 1,2-dimethylenecyclobutanes is disclosed (see scheme; TMS = trimethylsilyl). The mechanism of the reaction has been investigated by deuterium labeling experiments and the selectivity has been studied by DFT calculations.

Bacterial cell leakage potential of newly synthesized quinazoline derivatives of 1,5-benzodiazepines analogue

Dwivedi, Jaya,Kishore, Dharma,Misra, Apoorva,Sharma, Swapnil,Shukla, Shruti

, (2020/02/13)

Novel quinazoline embellished analogues of 1,5-benzodiazepine (6, 9, 13, 17, 21 and 24) were synthesized using one-pot domino approach. Structure of the compounds synthesized, were established with the help of IR, 1H NMR, 13C NMR and

βUnsaturated acyl cyanides as new bis-electrophiles for enantioselective organocatalyzed formal [3+3]spiroannulation

Goudedranche, Sebastien,Bugaut, Xavier,Constantieux, Thierry,Bonne, Damien,Rodriguez, Jean

supporting information, p. 410 - 415 (2014/04/03)

α,β-Unsaturated acyl cyanides are key bis-electrophile substrates for successful domino enantioselective organocatalyzed Michael-intramolecular acylation domino sequences. This new reactivity has been applied to the synthesis of enantioenriched azaspiro[4

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