3-Hydroxyhippuricacid
- Name 3-Hydroxyhippuricacid
- CAS 1637-75-8
- Purity 99%
Product Details
Chinese Factory Supply Wholesale 3-Hydroxyhippuricacid 1637-75-8 with Cheap Price
- Molecular Formula: C9H9NO4
- Molecular Weight: 195.175
- Vapor Pressure: 2.08E-10mmHg at 25°C
- Melting Point: 185 °C(Solv: water (7732-18-5))
- Refractive Index: 1.604
- Boiling Point: 489.8 °C at 760 mmHg
- PKA: 3.70±0.10(Predicted)
- Flash Point: 250 °C
- PSA： 90.12000
- Density: 1.4g/cm3
- LogP: 0.78140
3-Hydroxyhippuricacid(Cas 1637-75-8) Usage
|
Definition |
ChEBI: An N-acylglycine that is hippuric acid (N-benzoylglycine) substituted at position 3 on the phenyl ring by a hydroxy group. |
InChI:InChI=1/C9H9NO4/c11-7-3-1-2-6(4-7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)
1637-75-8 Relevant articles
Discovery of N-(2-(Benzylamino)-2-oxoethyl)benzamide analogs as a novel scaffold of pancreatic β-cell protective agents against endoplasmic reticulum stress
Eeda, Venkateswararao,Herlea-Pana, Oana,Lim, Hui-Ying,Wang, Weidong
, p. 388 - 393 (2020/01/02)
Endoplasmic reticulum (ER) stress-induce...
Development of a QuEChERS-Based Stable-Isotope Dilution LC-MS/MS Method to Quantitate Ferulic Acid and Its Main Microbial and Hepatic Metabolites in Milk
Waterstraat, Martin,Hildebrand, Andreas,Rosler, Margit,Bunzel, Mirko
, p. 8667 - 8677 (2016/11/29)
Forage plants of the Poaceae family are ...
Crystal structure of the Homo sapiens kynureninase-3-hydroxyhippuric acid inhibitor complex: Insights into the molecular basis of kynureninase substrate specificity
Lima, Santiago,Kumar, Sunil,Gawandi, Vijay,Momany, Cory,Phillips, Robert S.
experimental part, p. 389 - 396 (2009/10/01)
Homo sapiens kynureninase is a pyridoxal...
Substrate Specificity and Stoichiometry of Nα-Benzyloxycarbonyl Amino Acid Urethane Hydrolase from Streptococcus faecalis R ATCC 8043
Matsumura, Eiko,Shin, Takashi,Murao, Sawao,Kawano, Tatsu
, p. 973 - 980 (2007/10/02)
The substrate specificity of a new enzym...
1637-75-8 Process route
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99-06-9
3-Carboxyphenol
-
-
1637-75-8
(3-hydroxybenzamido)acetic acid
| Conditions | Yield |
|---|---|
|
Multi-step reaction
with
4
steps
1: triethylamine / 16 h / 60 °C
2: thionyl chloride / acetone / 2 h / 0 °C
3: sodium hydroxide / toluene; water / 5 h / 0 - 20 °C
4: acetic acid / water; acetonitrile
With
thionyl chloride; acetic acid; triethylamine; sodium hydroxide;
In
water; acetone; toluene; acetonitrile;
|
|
|
Multi-step reaction
with
2
steps
1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0 - 20 °C
2: lithium hydroxide / ethanol
With
benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide;
In
ethanol; N,N-dimethyl-formamide;
|
-
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586-38-9
3-Methoxybenzoic acid
-
-
1637-75-8
(3-hydroxybenzamido)acetic acid
| Conditions | Yield |
|---|---|
|
Multi-step reaction
with
2
steps
1: 30 percent / chloroethylcarbonate / tetrahydrofuran
2: 15 percent
With
chloromethylmethylcarbonate;
In
tetrahydrofuran;
|
1637-75-8 Upstream products
-
20938-64-1
N-(3-Aminobenzoyl)glycine
-
623-33-6
glycine ethyl ester hydrochloride
-
16446-73-4
3-(chlorocarbonyl)phenyl acetate
-
1211-92-3
methyl 2-(3-methoxybenzamido)acetate
1637-75-8 Downstream products
-
109866-43-5
2-(3-acetoxy-phenyl)-4-(4-dimethylamino-benzylidene)-4H -oxazol-5-one
-
56-40-6
glycine
-
99-06-9
3-Carboxyphenol
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