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Used in Pharmaceutical Industry:
L-Tyrosine, 3,5-dibroMo-, Methyl ester, hydrochloride (1:1) is used as an intermediate in the synthesis of drugs for the treatment of various medical conditions, such as cancer and neurological disorders. Its unique structure allows for the development of targeted therapies with potential applications in these fields.
Used in Neuroscience Research:
In the field of neuroscience, L-Tyrosine, 3,5-dibroMo-, Methyl ester, hydrochloride (1:1) serves as a biochemical tool, aiding in the study of protein structure and function. Its role in this area is crucial for advancing our understanding of complex biological processes and the development of novel therapeutic strategies.
Used in Chemical Synthesis:
L-Tyrosine, 3,5-dibroMo-, Methyl ester, hydrochloride (1:1) is also used as a building block in the synthesis of various chemical compounds for research purposes. Its versatility in chemical reactions makes it a valuable component in the creation of new molecules with potential applications in various industries.

61039-29-0

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61039-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61039-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,3 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61039-29:
(7*6)+(6*1)+(5*0)+(4*3)+(3*9)+(2*2)+(1*9)=100
100 % 10 = 0
So 61039-29-0 is a valid CAS Registry Number.

61039-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dibromotyrosine methyl ester hydrochloride

1.2 Other means of identification

Product number -
Other names (S)-Methyl 2-amino-3-(3,5-dibromo-4-hydroxyphenyl)propanoate hydrochloride

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:61039-29-0 SDS

61039-29-0Relevant academic research and scientific papers

SYNTHESIS OF PIPERAZINOMYCIN, A NOVEL ANTIFUNGAL ANTIBIOTIC

Nishiyama, Shigeru,Nakamura, Kazuhiko,Suzuki, Yoshikazu,Yamamura, Shosuke

, p. 4481 - 4484 (2007/10/02)

Piperazinomycin, a novel antifungal antibiotic, has been synthesized from tetrabromotyrosyltyrosine, whose oxidation with thallium trinitrate (TTN) leads to the formation of a strained 14-membered ring similar to that of piperazinomycin as a key step.

ATTOGRAM-LEVEL DETECTION AND RELATIVE RESPONSE OF STRONG ELECTROPHORES BY GAS CHROMATOGRAPHY WITH ELECTRON CAPTURE DETECTION.

Corkill,Joppich,Kuttab,Giese

, p. 481 - 485 (2007/10/02)

The responses as peak areas of some divergent compounds, most of which are strong electron absorbers, are measured by gas chromatography with electron capture detection (GC-ECD). The most sensitive compounds are derivatized lodothyronines, which are essentially 20-fold more sensitive than lindane. N,N-Dipentafluorobenzoylpentafluoroaniline, a somewhat less sensitive but more volatile substance, was selected for determination of a detection limit. The value was 90 ag(1. 6 multiplied by 10** minus **1**9 mol), largely due to an anomalous increase in its response at the trace level. This increases the reported sensitivity of GC-ECD by 100-fold.

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