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BOC-HYP-OH, also known as Nα-BOC-L-hydroxyproline, is a synthetic derivative of the amino acid hydroxyproline. It is commonly used in peptide synthesis as a protective group for hydroxyproline residues, allowing for selective modifications of peptides. BOC-HYP-OH is often employed in the production of collagen-based biomaterials, as well as in the development of pharmaceuticals and other bioactive compounds. This chemical plays a crucial role in the field of organic chemistry and biochemistry, facilitating the creation of complex peptides and molecules with specific properties and functions.

331442-12-7

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  • 1,2-Pyrrolidinedicarboxylicacid, 4-hydroxy-, 1-(1,1-dimethylethyl) ester, (2S)-

    Cas No: 331442-12-7

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331442-12-7 Usage

Uses

Used in Peptide Synthesis:
BOC-HYP-OH is used as a protective group for hydroxyproline residues in peptide synthesis, enabling selective modifications of peptides. This allows for the creation of complex peptides with specific properties and functions.
Used in Production of Collagen-based Biomaterials:
BOC-HYP-OH is used in the production of collagen-based biomaterials, contributing to the development of advanced materials with unique properties and applications in various industries.
Used in Pharmaceutical Development:
BOC-HYP-OH is utilized in the development of pharmaceuticals and other bioactive compounds, playing a crucial role in the synthesis of therapeutic agents with specific biological activities.
Used in Organic Chemistry and Biochemistry Research:
BOC-HYP-OH is employed in research within the fields of organic chemistry and biochemistry, facilitating the exploration of new chemical reactions and the synthesis of novel compounds with potential applications in various areas.

Check Digit Verification of cas no

The CAS Registry Mumber 331442-12-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,4,4 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 331442-12:
(8*3)+(7*3)+(6*1)+(5*4)+(4*4)+(3*2)+(2*1)+(1*2)=97
97 % 10 = 7
So 331442-12-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO5/c1-10(2,3)16-9(15)11-5-6(12)4-7(11)8(13)14/h6-7,12H,4-5H2,1-3H3,(H,13,14)

331442-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (trans)-1-[(1,1-dimethylethoxy)carbonyl]-4-hydroxy-L-proline

1.2 Other means of identification

Product number -
Other names N-(tert-butoxycarbonyl)-L-4-hydroxyproline

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:331442-12-7 SDS

331442-12-7Relevant articles and documents

Methods for modulating phototoxicity

-

Page 4, (2008/06/13)

The invention relates to methods for modulating photodamage via the use of collagen derived molecules which either enhance or inhibit damage caused by ultraviolet light.

Pyrrolidylthiocarbapenem derivative

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, (2008/06/13)

A pyrrolidylthiocarbapenem derivative represented by Formula I is provided: STR1 wherein R1 is hydrogen or lower alkyl; R2, R3 and R4 are hydrogen, lower alkyl which can be substituted or an amino protecting group independently, or R2 and R3 together with a nitrogen atom to which R2 and R3 are bonded form a saturated or unsaturated cyclic group, or R2 and R4, or R3 and R4 together with two nitrogen atoms and one sulfur atom in the sufamide group form a saturated or unsaturated cyclic group; each cyclic group can further include at least one atom selected from the group consisting of oxygen, sulfur and nitrogen, and each cyclic group can be substituted; X1 is hydrogen or a hydroxy protecting group; X2 is hydrogen, a carboxy protecting group, an ammonio group, an alkali metal or an alkaline-earth metal; and Y2 is hydrogen or an amino protecting group.

SUBSTITUTED 4-PHENOXY OR 4-PHENYLTHIO PROLINES

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, (2008/06/13)

This invention is directed to substituted 4-phenoxy and 4-phenylthio prolines of the formula STR1 which possess useful hypotensive activity.

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