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89536-85-6

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89536-85-6 Usage

Description

BOC-D-MEVAL-OH, also known as tert-butyloxycarbonyl-D-mevalonic acid, is a chemical compound derived from mevalonic acid, a key intermediate in the biosynthesis of isoprenoids and sterols. It is commonly used in organic synthesis and biochemical research, serving as a building block for the creation of complex organic molecules. Notably, BOC-D-MEVAL-OH is used to protect amino groups in peptide synthesis and is a precursor in the production of pharmaceuticals, agrochemicals, and other biologically active compounds. It is also used as a reagent in the preparation of various organic compounds and is available as a white crystalline powder with a molecular weight of 278.32 g/mol.

Uses

Used in Organic Synthesis:
BOC-D-MEVAL-OH is used as a building block for the creation of complex organic molecules, contributing to the development of new compounds with potential applications in various industries.
Used in Biochemical Research:
BOC-D-MEVAL-OH is utilized as a reagent in biochemical research, aiding in the study of isoprenoids and sterols, which are essential components of various biological processes.
Used in Pharmaceutical Production:
BOC-D-MEVAL-OH is used as a precursor in the production of pharmaceuticals, playing a crucial role in the synthesis of biologically active compounds that can be used for the treatment of various diseases and conditions.
Used in Agrochemical Production:
BOC-D-MEVAL-OH is also used as a precursor in the production of agrochemicals, contributing to the development of compounds that can enhance crop yield and protect plants from pests and diseases.
Used in Peptide Synthesis:
BOC-D-MEVAL-OH is used to protect amino groups during peptide synthesis, ensuring the successful formation of desired peptide sequences and facilitating the development of peptide-based drugs and therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 89536-85-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,3 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89536-85:
(7*8)+(6*9)+(5*5)+(4*3)+(3*6)+(2*8)+(1*5)=186
186 % 10 = 6
So 89536-85-6 is a valid CAS Registry Number.

89536-85-6 Well-known Company Product Price

  • Brand
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  • Detail
  • Alfa Aesar

  • (H62443)  N-Boc-N-methyl-D-valine, 95%   

  • 89536-85-6

  • 250mg

  • 242.0CNY

  • Detail
  • Alfa Aesar

  • (H62443)  N-Boc-N-methyl-D-valine, 95%   

  • 89536-85-6

  • 1g

  • 726.0CNY

  • Detail
  • Alfa Aesar

  • (H62443)  N-Boc-N-methyl-D-valine, 95%   

  • 89536-85-6

  • 5g

  • 2906.0CNY

  • Detail

89536-85-6SDS

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 (R)-2-((tert-Butoxycarbonyl)(methyl)amino)-3-methylbutanoic acid

1.2 Other means of identification

Product number -
Other names (2R)-3-methyl-2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]butanoic 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:89536-85-6 SDS

89536-85-6Downstream Products

89536-85-6Relevant articles and documents

First total synthesis of hoshinoamide A

Liu, Long,Rui, Zihan,Shao, Yutian,Xu, Shengtao,Yang, Yiming,Zhou, Haipin

supporting information, p. 2924 - 2931 (2022/01/12)

Hoshinoamides A, B and C, linear lipopeptides, were isolated from the marine cyanobacterium Caldora penicillata, with potent antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum. Herein, we describe the first total synthesis of hosh

Solution-phase synthesis and biological evaluation of triostin A and its analogues

Hattori, Kozo,Koike, Kota,Okuda, Kensuke,Hirayama, Tasuku,Ebihara, Masahiro,Takenaka, Mei,Nagasawa, Hideko

supporting information, p. 2090 - 2111 (2016/02/18)

Triostin A is a biosynthetic precursor of echinomycin which is one of the most potent hypoxia inducible factor 1 (HIF-1) inhibitors. An improved solution-phase synthesis of triostin A on a preparative scale has been achieved in 17.5% total yield in 13 ste

Total synthesis, absolute configuration, and biological activity of xyloallenoide A

Wang, San-Yong,Xu, Zhong-Liang,Wang, Hui,Li, Chun-Rong,Fu, Li-Wu,Pang, Ji-Yan,Li, Jing,She, Zhi-Gang,Lin, Yong-Cheng

experimental part, p. 973 - 982 (2012/08/08)

The novel natural product xyloallenoide A, isolated from the marine mangrove endophytic fungus from the South China Sea, and its diastereoisomer xyloallenoide A1, which contain N-methyl-substituted amino acids, were synthesized. The absolute configurations of the amino acid units of xyloallenoide A were finally confirmed to be L-Lys, Me-D-Val, and Me-L-Ala. This report represents a practical and attractive alternative for the synthesis of N-methyl-substituted cyclotripeptides. In the preliminary bioassay, synthetic xyloallenoide A showed marginal activities against KB (IC50=9.6 mm) and KBv200 cells (IC50=10.3 μm), and xyloallenoide A1 was inactive against KB and KBv200 cells.

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