- CAS
- Purity
- 7743-39-7
- 99%
Factory supply 3,5-bis(acetylamino)benzoic acid 7743-39-7 with sufficient stock and high standard
- Molecular Formula:C11H12N2O4
- Molecular Weight:236.227
- Vapor Pressure:1.68E-14mmHg at 25°C
- Boiling Point:584.4°C at 760 mmHg
- Flash Point:307.2°C
- PSA：95.50000
- LogP:1.44760
3,5-bis(acetylamino)benzoic acid(Cas 7743-39-7) Usage
|
General Description |
3,5-bis(acetylamino)benzoic acid, also known as N-acetylgalactosamine, is a chemical compound with the molecular formula C14H15N3O6. It is a derivative of benzoic acid and is commonly used in biochemistry and organic synthesis. 3,5-bis(acetylamino)benzoic acid is often used as a building block for the synthesis of complex organic molecules and is an important intermediate in the production of various pharmaceuticals and organic compounds. It is also a key component of glycosaminoglycans, which are essential for the formation of connective tissues in the human body. Additionally, 3,5-bis(acetylamino)benzoic acid is a valuable tool for studying carbohydrate-protein interactions and is a key component in the development of new and improved drugs for various medical conditions. |
InChI:InChI=1/C11H12N2O4/c1-6(14)12-9-3-8(11(16)17)4-10(5-9)13-7(2)15/h3-5H,1-2H3,(H,12,14)(H,13,15)(H,16,17)/p-1
7743-39-7 Relevant articles
Water soluble lanthanoid benzoate complexes for the kinetic separation of cis/trans-limonene oxide
Andrews, Philip C.,Blair, Michael,Fraser, Benjamin H.,Junk, Peter C.,Massi, Massimiliano,Tuck, Kellie L.
, p. 2833 - 2838 (2007/10/03)
A new class of water soluble, environmen...
O2 and CO Binding Behavior of Double-Sided Porphyrinatoiron(II) Complexes Modified by Amide Residues
Komatsu, Teruyuki,Kumamoto, Shin-ichi,Nishide, Hiroyuki,Tsuchida, Eishun
, p. 1640 - 1646 (2007/10/02)
New double-sided porphyrinatoiron(II) co...
H-bonded oxyhemoglobin models with substituted picket-fence porphyrins: The model compound equivalent of site-directed mutagenesis
Wuenschell, Gerald E.,Tetreau, Catherine,Lavalette, Daniel,Reed, Christopher A.
, p. 3346 - 3355 (2007/10/02)
Iron(II) complexes of picket-fence-type ...
7743-39-7 Process route
-
-
535-87-5
3.5-diaminobenzoic acid
-
-
75-36-5
acetyl chloride
-
-
7743-39-7
3,5-bis(acetamido)benzoic acid
Conditions
| Conditions | Yield |
|---|---|
|
With
pyridine;
In
diethyl ether;
at 0 ℃;
for 1h;
|
73% |
|
With
sodium hydroxide;
for 2h;
Yield given;
Ambient temperature;
|
-
-
535-87-5
3.5-diaminobenzoic acid
-
-
108-24-7
acetic anhydride
-
-
7743-39-7
3,5-bis(acetamido)benzoic acid
Conditions
| Conditions | Yield |
|---|---|
|
With
potassium carbonate;
In
water;
at 20 ℃;
|
91% |
7743-39-7 Upstream products
-
535-87-5
3.5-diaminobenzoic acid
-
75-36-5
acetyl chloride
-
108-24-7
acetic anhydride
7743-39-7 Downstream products
-
139870-31-8
meso-mono<α-o-(3,5-diacetamidobenzenecarboxamido)phenyl>tris(α,α,α-o-pivalamidophenyl)porphyrin
-
1713-07-1
2,4,6,triiodo-5-amino-3-acetylaminobenzoic acid