Login   |   Create New Account sales@aaronchem.com

Home > Products> 61535-46-4
61535-46-4

3-BENZYLOXY-BENZOYL CHLORIDE

Catalog#: AR003JNX  |   CAS#: 61535-46-4  |   MDL#: MFCD02258040  |   MF: C14H11ClO2  |   MW: 246.68893999999997

Packsize Purity Price Availability Quantity
100mg 98% $49.00 Global Stock Buy Now Add To Cart
250mg 98% $77.00 Global Stock Buy Now Add To Cart
1g 98% $250.00 Global Stock Buy Now Add To Cart
  • Description
  • Application
  • Related Products
  • Featured Products
Catalog Number AR003JNX
Chemical Name 3-BENZYLOXY-BENZOYL CHLORIDE
CAS Number 61535-46-4
Molecular Formula C14H11ClO2
Molecular Weight 246.68893999999997
MDL Number MFCD02258040
SMILES ClC(=O)c1cccc(c1)OCc1ccccc1

3-BENZYLOXY-BENZOYL CHLORIDE is a versatile compound widely used in chemical synthesis as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a valuable building block for the synthesis of complex organic molecules due to its unique reactivity and structural properties.One common application of 3-BENZYLOXY-BENZOYL CHLORIDE is in the synthesis of benzophenone derivatives, which have a wide range of industrial and pharmaceutical applications. By reacting with nucleophiles such as amines, alcohols, or thiols, 3-BENZYLOXY-BENZOYL CHLORIDE can undergo nucleophilic substitution reactions to introduce functional groups at specific positions on the benzophenone scaffold.Additionally, 3-BENZYLOXY-BENZOYL CHLORIDE is often utilized in the preparation of esters and amides through acylation reactions. By reacting with various alcohols or amines in the presence of a base or acid catalyst, this compound can facilitate the formation of ester or amide bonds, allowing for the synthesis of diverse chemical compounds with tailored properties.Furthermore, 3-BENZYLOXY-BENZOYL CHLORIDE can also participate in cross-coupling reactions with organometallic reagents, such as Grignard reagents or organolithium compounds, to form biaryl compounds or other complex organic structures. These cross-coupling reactions enable the efficient construction of carbon-carbon bonds, crucial for the synthesis of intricate molecular architectures.Overall, the versatile reactivity and functional group compatibility of 3-BENZYLOXY-BENZOYL CHLORIDE make it a valuable reagent in chemical synthesis, enabling the efficient and controlled assembly of diverse organic compounds with potential applications in various industrial sectors.
1486-50-6

Benzoyl chloride, 4-(phenylmethoxy)-

1486-50-6

130205-11-7

Benzaldehyde, 3-(1-naphthalenylmethoxy)-

130205-11-7

61535-46-4

3-BENZYLOXY-BENZOYL CHLORIDE

61535-46-4

1700-37-4

3-Benzyloxybenzaldehyde

1700-37-4

24033-03-2

m-(Benzyloxy)benzyl Chloride

24033-03-2

40359-58-8

3-[(4-Methylbenzyl)oxy]benzaldehyde

40359-58-8

214847-64-0

Benzoyl chloride, 3-(1-methylethoxy)- (9CI)

214847-64-0

136996-42-4

3-[(3-Chlorobenzyl)oxy]benzoyl chloride

136996-42-4

851077-04-8

4-(benzyloxy)naphthalene-2-carbaldehyde

851077-04-8

1314538-55-0

Borate(1-), [[[(1,1-dimethylethoxy)carbonyl]amino]methyl]trifluoro-, potassium (1:1), (T-4)-

1314538-55-0

$4.00/100mg, $4.00/250mg, $15.00/1g, $51.00/5g, $89.00/10g, $171.00/25g, $326.00/50g, $511.00/100g,

1377503-12-2

Phenol, 5-​chloro-​2-​(4,​4,​5,​5-​tetramethyl-​1,​3,​2-​dioxaborolan-​2-​yl)​-

1377503-12-2

$22.00/250mg, $52.00/1g, $174.00/5g, $312.00/10g, $779.00/25g,

875781-43-4

2-Bromo-5H-pyrrolo[2,3-b]pyrazine

875781-43-4

$4.00/250mg, $7.00/1g, $21.00/5g, $40.00/10g, $99.00/25g, $364.00/100g,

67400-25-3

3-Bromo-5-nitroindazole

67400-25-3

$5.00/1g, $11.00/5g, $20.00/10g, $43.00/25g, $84.00/50g, $134.00/100g, $667.00/500g,

21575-91-7

Benzenepropanoic acid,3-bromo-b-oxo-, ethyl ester

21575-91-7

$4.00/250mg, $9.00/1g, $39.00/5g, $66.00/10g, $139.00/25g, $433.00/100g,

Home| Products| Terms & Conditions| Ordering & Shipping| Company| Contact us

© 2019 Aaron Chemicals LLC. All Rights Reserved.