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3-N-BOC-AMINO-4,4-DIMETHYL PENTANOIC ACID is a chemical compound characterized by a five-carbon chain with a carboxylic acid group and a BOC-protected amino group at the third position, along with two methyl groups at the fourth carbon. 3-N-BOC-AMINO-4,4-DIMETHYL PENTANOIC ACID is known for its role in organic synthesis, especially in the production of peptide and amino acid derivatives, due to its selective reactivity and the protective nature of the BOC group.

856417-59-9

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856417-59-9 Usage

Uses

Used in Organic Synthesis:
3-N-BOC-AMINO-4,4-DIMETHYL PENTANOIC ACID is used as a building block in organic synthesis for the creation of complex molecules. The BOC-protected amino group allows for selective reactions with other functional groups, which is crucial for the synthesis of intricate organic compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 3-N-BOC-AMINO-4,4-DIMETHYL PENTANOIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals. The carboxylic acid group present in the compound is particularly useful for forming esters and amides, which are common structural elements in many drugs.
Used in Specialty Chemicals Production:
3-N-BOC-AMINO-4,4-DIMETHYL PENTANOIC ACID is also utilized in the production of specialty chemicals, where its unique structure and functional groups contribute to the development of high-value chemical products with specific applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 856417-59-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,4,1 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 856417-59:
(8*8)+(7*5)+(6*6)+(5*4)+(4*1)+(3*7)+(2*5)+(1*9)=199
199 % 10 = 9
So 856417-59-9 is a valid CAS Registry Number.

856417-59-9SDS

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 3-((tert-Butoxycarbonyl)amino)-4,4-dimethylpentanoic acid

1.2 Other means of identification

Product number -
Other names 4,4-dimethyl-3-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic 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:856417-59-9 SDS

856417-59-9Downstream Products

856417-59-9Relevant academic research and scientific papers

UREA DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE

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Page/Page column 59-60, (2010/11/23)

The present invention provides a urea derivative or a salt thereof, which is useful as a therapeutic agent for thrombosis. The derivative is represented by Formula (I): [Chemical formula I] wherein Cy is an aromatic hydrocarbon group which may be substituted or an aromatic heterocyclic group which may be substituted; R1 is a hydrogen atom or a hydrocarbon group which may be substituted; V is -C(O)-, -S(O)-, or -S(O)2-; W is -N(R2)-, -O-, or a bond (wherein R2 is a hydrogen atom or a hydrocarbon group which may be substituted); X is alkylene which may be substituted; Y is -C(O)-, -S(O)-, or -S(O)2-; Z is a bond, a chain hydrocarbon group which may be substituted, or -N=; ring A is a non-aromatic nitrogen-containing heterocyclic ring which may be substituted; ring B is a nitrogen-containing heterocyclic ring which may be substituted; and [Chemical formula 2]------ ̄?,?------? are each independently a single bond or a double bond; provided that R1 may be bonded to R2 to form a non-aromatic nitrogen-containing heterocyclic ring and that R2 may be bonded to a substituent of X to form a non-aromatic nitrogen-containing heterocyclic ring which may be substituted.

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