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157698-32-3

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157698-32-3 Usage

Chemical Properties

Pale Brown Cyrstals

Uses

Different sources of media describe the Uses of 157698-32-3 differently. You can refer to the following data:
1. A labelled, nonsteroidal estrogen antagonist of interest in the treatment of some forms of breast cancer
2. Labelled Tamoxifen (T006000). A nonsteroidal estrogen antagonist of interest in the treatment of some forms of breast cancer. Tamoxifen is a protein kinase C inhibitor, and induces apoptosis in human malignant glioma cell lines.

Check Digit Verification of cas no

The CAS Registry Mumber 157698-32-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,6,9 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 157698-32:
(8*1)+(7*5)+(6*7)+(5*6)+(4*9)+(3*8)+(2*3)+(1*2)=183
183 % 10 = 3
So 157698-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C26H29NO/c1-4-25(21-11-7-5-8-12-21)26(22-13-9-6-10-14-22)23-15-17-24(18-16-23)28-20-19-27(2)3/h5-18H,4,19-20H2,1-3H3/b26-25-/i1D3,4D2

157698-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-2-[4-[(Z)-3,3,4,4,4-pentadeuterio-1,2-diphenylbut-1-enyl]phenoxy]ethanamine

1.2 Other means of identification

Product number -
Other names (E/Z)-Mammaton-d5

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:157698-32-3 SDS

157698-32-3Downstream Products

157698-32-3Relevant articles and documents

Synthesis of -tamoxifen; A Mechanistic Probe of Tamoxifen Induced Hepatic DNA Adduct Formation

Horton, Martin N.,Jarman, Michael,Potter, Gerard A.

, p. 767 - 772 (1994)

Tamoxifen which incorporates a fully deuterated ethyl group, 5-ethyl>-tamoxifen, has been synthesised in order to probe the mechanism of tamoxifen induced hepatic DNA adduct formation.The pentadeuteroethyl group was introduced into the tamoxi

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