ChemicalBook >> CAS DataBase List >>Zofenopril

Zofenopril

CAS No.
81872-10-8
Chemical Name:
Zofenopril
Synonyms
NAA;NAA(R);NAA(TM);ALPHA-NAA;Zofenopril;ROOTONE(R);FRUIT FAX(R);Zofenopril-d5;AKOS AU36-M588;RARECHEM AL BO 0198
CBNumber:
CB1679843
Molecular Formula:
C22H23NO4S2
Molecular Weight:
429.55
MDL Number:
MFCD00870957
MOL File:
81872-10-8.mol
Last updated:2023-06-25 18:02:04

Zofenopril Properties

Melting point 129-131.5 °C(lit.)
alpha D25 -36.5° (c = 1 in methanol)
Boiling point 646.3±55.0 °C(Predicted)
Density 1.34±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO: 5 mg/mL (11.64 mM)
form crystalline
pka pK1:4.236 (25°C)
color light yellow
CAS DataBase Reference 81872-10-8(CAS DataBase Reference)
FDA UNII 290ZY759PI
ATC code C09AA15

SAFETY

Risk and Safety Statements

Hazard Codes  Xn,Xi
Risk Statements  22-37/38-41
Safety Statements  23-24/25
WGK Germany  3
RTECS  QJ0875000
HazardClass  IRRITANT

Zofenopril price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-7911 Zofenopril 98.81% 81872-10-8 5mg $192 2021-12-16 Buy
American Custom Chemicals Corporation RDL0007209 ZOFENOPRIL-D5 95.00% 81872-10-8 5MG $502.66 2021-12-16 Buy
CSNpharm CSN21981 Zofenopril 81872-10-8 5mg $163 2021-12-16 Buy
Product number Packaging Price Buy
CS-7911 5mg $192 Buy
RDL0007209 5MG $502.66 Buy
CSN21981 5mg $163 Buy

Zofenopril Chemical Properties,Uses,Production

Originator

Zofenopril Calcium,ZYF Pharm Chemical

Uses

Zofenopril-d5 is intended for use as an internal standard for the quantification of Zofenopril by GC- or LC-mass spectrometry.

Definition

ChEBI: A proline derivative that is 4-(phenylsulfanyl)-L-proline in which the amine proton is replaced by a (2S)-3-(benzoylsulfanyl)-2-methylpropanoyl group. A prodrug for zofenoprilat.

Manufacturing Process

9.9 g (0.031 mole) of cis-4-phenylthio-L-proline is suspended in 100 ml of water (pH 5.6) and the pH is adjusted to 10.2 by the addition of about 20 ml of 10% sodium bicarbonate to provide a clear solution. The pH is then adjusted to 9.5 by the addition of about 4.5 ml of concentrated HCl. The solution is kept at 30°C while 8.1 g (0.033 mole) of (D)-3-(benzoylthio)-2- methylpropanoic acid chloride in 30 ml of toluene is added simultaneously with 100 ml of 10% sodium bicarbonate to keep the pH at 9.3. After about 1/4 of the acid chloride is added, a slimy precipitate begins to form which persists throughout the reaction. After stirring the reaction mixture at pH 9.3 for 2.5 h, it is made strongly acidic by adding 20% HCl in the presence of ethyl acetate. The aqueous layer is extracted twice with 350 ml portions of ethyl acetate and the combined organic layers are washed with 300 ml of saturated brine and dried (MgSO 4 ). The solvent is removed to yield 11.8 g of foamy solid cis-1-[D-3-(benzoylthyo)-2-methyl-1-oxopropyl]-4-(phenylthio)-L-proline hydrochloride.
To a solution of this cis-1-[D-3-(benzoylthyo)-2-methyl-1-oxopropyl]-4- (phenylthio)-L-proline hydrochloride 11.8 g (0.027 mole) in 70 ml of acetonitrile there is added about 6.0 g of dicyclohexylamine in 25 ml of ether. A white crystalline precipitate forms immediately. After standing overnight in the cold room, the solid is filtered and washed with ether to yield (cis)-1-[D- 3-(benzoylthio)-2-methyl-1-oxopropyl]-4-(phenylthio)-L-proline, dicyclohexylamine salt (1:1).
he slightly moist (cis)-1-[D-3-(benzoylthio)-2-methyl-1-oxopropyl]-4- (phenylthio)-L-proline dicyclohexylamine salt is stirred for 2.5 h in a mixture of 300 ml of ethyl acetate and 200 ml of 10% potassium bisulfate. Two clear layers form. The aqueous layer is extracted with two 200 ml portions of ethyl acetate and the combined organic layers are dried (MgSO 4 ). The solvent is removed to yield 10.1 g of foamy solid (cis)-1-[D-3-(benzoylthio)-2-methyl-1- oxopropyl]-4-(phenylthio)-L-proline; melting point 42-44°C.
In practice it is usually used as calcium salt (2:1).

brand name

Zoprace (Bristol-Myers Squibb).

Therapeutic Function

Antihypertensive

Synthesis Reference(s)

The Journal of Organic Chemistry, 33, p. 1675, 1968 DOI: 10.1021/jo01268a091

105107-84-4
74654-91-4
81872-10-8
Synthesis of Zofenopril from cis-4-Phenylthio-L-proline hydrochloride and S-benzoyl-3-mercapto-2-methylpropanoyl chloride
Global( 136)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Guanlang Biotechnology Co,.LTD
+8619930503252 daisy@crovellbio.com China 5964 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
WinWin Chemical CO., Limited
+86-0086-577-64498589 +86-15355981851 sales@win-winchemical.com China 13854 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9358 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29271 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418684 +8618949823763 sales@tnjchem.com China 25363 58
ZHEJIANG JIUZHOU CHEM CO., LTD
+86-0576225566889 +86-13454675544 admin@jiuzhou-chem.com;jamie@jiuzhou-chem.com;alice@jiuzhou-chem.com China 20000 58
Hu Bei Jiutian Bio-medical Technology CO.,Ltd
027-88013699 17354350817 Ryan@jiutian-bio.com China 7433 58

Related articles

View Lastest Price from Zofenopril manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Zofenopril pictures 2023-06-26 Zofenopril
81872-10-8
US $5.00-2.00 / KG 1KG 99% 10000kg Hebei Guanlang Biotechnology Co,.LTD
Zofenopril-d5 pictures 2023-04-12 Zofenopril-d5
81872-10-8
US $1.00 / kg 1kg 99% 2000tons/year Wuhan Dujiang Industrial Co., Ltd.
Zofenopril-d5 USP/EP/BP pictures 2021-08-11 Zofenopril-d5 USP/EP/BP
81872-10-8
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited
  • Zofenopril pictures
  • Zofenopril
    81872-10-8
  • US $5.00-2.00 / KG
  • 99%
  • Hebei Guanlang Biotechnology Co,.LTD
  • Zofenopril-d5 pictures
  • Zofenopril-d5
    81872-10-8
  • US $1.00 / kg
  • 99%
  • Wuhan Dujiang Industrial Co., Ltd.
1-NAPHTHYLACETICACIDα-NAPHTHYLACETICACID 1-[(S)-3-(Benzoylthio)-2-methyl-1-oxopropyl]-4α-(phenylthio)-L-proline S-Benzoyl-4-phenylthiocaptopril (4S)-N-[3-(Benzoylsulfanyl)-2(S)-methylpropionyl]-4-(phenylsulfanyl)-L-proline Zofenopril NAA(R) NAA(TM) NAA NAPHTHALENEACETIC ACID RARECHEM AL BO 0198 ROOTONE(R) (2S,4S)-1-[(2S)-2-methyl-3-phenylcarbonylsulfanyl-propanoyl]-4-phenylsulfanyl-pyrrolidine-2-carboxylic acid (2S,4S)-1-[(2S)-3-(benzoylsulfanyl)-2-methylpropanoyl]-4-phenylsulfanylpyrrolidine-2-carboxylic acid (2S,4S)-1-[(2S)-3-(benzoylthio)-2-methyl-propanoyl]-4-(phenylthio)proline Zofenopril-d5 FRUIT FAX(R) ALPHA-NAA AKOS AU36-M588 (2S,4S)-1-[(2S)-3-(benzoylthio)-2-methyl-1-oxopropyl]-4-(phenylthio)-2-pyrrolidinecarboxylic acid L-Proline, 1-[(2S)-3-(benzoylthio)-2-methyl-1-oxopropyl]-4-(phenylthio)-, (4S)- Zofenopril-d5 USP/EP/BP Zofenopril D5Q: What is Zofenopril D5 Q: What is the CAS Number of Zofenopril D5 Q: What is the storage condition of Zofenopril D5 Q: What are the applications of Zofenopril D5 (naphthalen-1-yl)acetic acid (1-naphthylacetic acid) 81872-10-8 C10H7CH2COOH Auxins Plant Growth Regulators