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2-tert-ButyloxycarbonylaMino-5-heptenoic Acid is a chemical compound characterized by its unique structure that features a tert-butyloxycarbonyl group, an amino group, and a 5-heptenoic acid chain. This organic molecule is known for its reactivity and potential applications in the synthesis of complex organic compounds.

119808-36-5

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119808-36-5 Usage

Uses

Used in Pharmaceutical Industry:
2-tert-ButyloxycarbonylaMino-5-heptenoic Acid is used as a reactant for the preparation of (-)-Amathaspiramide F, a bioactive compound with potential therapeutic properties. Its role in the synthesis process is crucial for the development of new drugs and pharmaceutical agents that can address various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 119808-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,0 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 119808-36:
(8*1)+(7*1)+(6*9)+(5*8)+(4*0)+(3*8)+(2*3)+(1*6)=145
145 % 10 = 5
So 119808-36-5 is a valid CAS Registry Number.

119808-36-5SDS

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 2-tert-butoxycarbonylamino-hept-6-enoic acid

1.2 Other means of identification

Product number -
Other names 2-tert-Butyloxycarbonylamino-5-heptenoic Acid

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:119808-36-5 SDS

119808-36-5Relevant academic research and scientific papers

Design, synthesis, and biological activity of boronic acid-based histone deacetylase inhibitors

Suzuki, Nobuaki,Suzuki, Takayoshi,Ota, Yosuke,Nakano, Tatsuya,Kurihara, Masaaki,Okuda, Haruhiro,Yamori, Takao,Tsumoto, Hiroki,Nakagawa, Hidehiko,Miyata, Naoki

experimental part, p. 2909 - 2922 (2010/01/16)

Guided by the proposed catalytic mechanism of histone deacetylases (HDACs), we designed and synthesized a series of boronic acid-based HDAC inhibitors bearing an R-amino acid moiety. In this series, compounds (S)-18, 20, and 21 showed potent HDAC-inhibito

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