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10448-84-7

10448-84-7

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10448-84-7 Usage

Uses

Different sources of media describe the Uses of 10448-84-7 differently. You can refer to the following data:
1. Anti-estrogen.
2. Nitromifene is a free base of Nitromifene Citrate (E/Z mixture) (N496700). Nitromifene citrate is a non-steroidal estrogen antagonist. It is structurally similar to Tamoxifen (T006000), which is a selective estrogen response modifier (SERM).

Check Digit Verification of cas no

The CAS Registry Mumber 10448-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10448-84:
(7*1)+(6*0)+(5*4)+(4*4)+(3*8)+(2*8)+(1*4)=87
87 % 10 = 7
So 10448-84-7 is a valid CAS Registry Number.
InChI:InChI=1/C27H28N2O4/c1-32-24-13-9-21(10-14-24)26(27(29(30)31)23-7-3-2-4-8-23)22-11-15-25(16-12-22)33-20-19-28-17-5-6-18-28/h2-4,7-16H,5-6,17-20H2,1H3/b27-26-

10448-84-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-[4-[(Z)-1-(4-methoxyphenyl)-2-nitro-2-phenylethenyl]phenoxy]ethyl]pyrrolidine

1.2 Other means of identification

Product number -
Other names Nitromifeno [INN-Spanish]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10448-84-7 SDS

10448-84-7Upstream product

10448-84-7Downstream Products

10448-84-7Related news

Characterization of mcf 7 breast cancer cell growth inhibition by the antiestrogen Nitromifene (cas 10448-84-7) (CI 628) and selected metabolites07/31/2019

Besides undergoing O-demethylation in vivo the triarylethylene antiestrogen nitromifene [1(4-(2-pyrrolidinylethoxy)phenyl)-1(4-methoxy)-phenyl-2-phenyl-2-nitroethene, 1] undergoes biotransformation via nitroreduction, ethene bond cleavage, and pyrrolidine ring oxidation affording ketone metaboli...detailed

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