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102-92-1,MFCD00000732
Catalog No.:AA00066H
102-92-1 | 2-Propenoyl chloride, 3-phenyl-
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  • Technical Information
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Technical Information
Catalog Number:
AA00066H
Chemical Name:
2-Propenoyl chloride, 3-phenyl-
CAS Number:
102-92-1
Molecular Formula:
C9H7ClO
Molecular Weight:
166.6043
MDL Number:
MFCD00000732
IUPAC Name:
(E)-3-phenylprop-2-enoyl chloride
InChI:
InChI=1S/C9H7ClO/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H/b7-6+
InChI Key:
WOGITNXCNOTRLK-VOTSOKGWSA-N
SMILES:
ClC(=O)C=Cc1ccccc1
EC Number:
203-065-5
UNII:
04L46S032W
NSC Number:
4683
Properties
Computed Properties
 
Complexity:
157  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1  
Exact Mass:
166.019g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
166.604g/mol
Monoisotopic Mass:
166.019g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1  

Synonyms
 
cinnamoyl chloride 
cinnamoyl chloride, (E)-isomer 
Cinnamoylchloride 
trans-Cinnamoyl chloride 
(2E)-3-phenylprop-2-enoyl chloride 
3-Phenyl-2-propenoyl chloride 
UNII-04L46S032W 
NSC 4683 
(E)-3-phenylprop-2-enoyl chloride 
(E)-3-Phenyl-2-propenoyl chloride 
.beta.-Phenylacryloyl chloride 
WOGITNXCNOTRLK-VOTSOKGWSA-N 
Cinnamoyl chloride 
MFCD00000732 
04L46S032W 
2-Propenoyl chloride, 3-phenyl-, (2E)- 
3-Phenylpropenoyl chloride 
Cinnamoyl chloride, 98%, predominantly trans 
beta-Phenylacryloyl chloride 
Cinnamoyl chlocide 
EINECS 203-065-5 
Trans-cinnamoylchloride 
2-Propenoyl chloride, 3-phenyl-, (E)- 
102-92-1 
3-Phenylacryloyl chloride 
Cinnamoyl chloride, 98% 
Benzeneacrylic acid chloride 
trans-cinnamic acid chloride 
SCHEMBL37935 
AC1NS591 
(2E)-3-phenylacryloyl chloride 
(E)-3-phenyl-acryloyl chloride 
2-Propenoyl chloride,3-phenyl- 
DTXSID3059264 
17082-09-6 
NSC4683 
NSC-4683 
ZINC1680031 
BBL011393 
SBB040621 
STL146496 
AKOS000121270 
[(2E)-3-phenylprop-2-enoyl]chloride 
RP17409 
RTR-000680 
trans-3-Phenylacryloyl chloride 
BC651782 
CJ-06257 
I423 
SC-26692 
AB1011438 
RT-000241 
TR-000680 
AM20060479 
CS-0006860 
P0133 
Cinnamic acid chloride 
A800646 
I01-1982 
Q-200858 
I14-45492 
F2190-0089 
cinnamaldehyde 
cinnamoylchlorid- 
C9H7ClO 
benzylideneacetyl chloride 
Cinnamoyl chloride, (E)- 
Cinnamic chloride 
C9-H7-Cl-O 
(2E)-3-Phenyl-2-propenoyl chloride 
CID5354261 
Cinnamoyl chloride, 98%, predominantly trans - 100G 100g 
(E)-cinnamoyl chloride 
2-Propenoyl chloride, 3-phenyl- 
Literature

Title: Synthesis and antitumor activity of lapathoside D and its analogs.

Journal: European journal of medicinal chemistry 20120701

Title: Three-component reactions of isocyanides, dialkyl acetylenedicarboxylates, and trans-cinnamoyl chlorides for the synthesis of highly functionalized 2-vinyl furans.

Journal: Molecular diversity 20120201

Title: [A synthesis of cinnamoyloxyisoflavones].

Journal: Bioorganicheskaia khimiia 20060101

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