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BOC-D-TYR(BZL)-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 63769-58-4 Structure
  • Basic information

    1. Product Name: BOC-D-TYR(BZL)-OH
    2. Synonyms: N-ALPHA-T-BOC-O-BENZYL-D-TYROSINE;N-ALPHA-T-BUTOXYCARBONYL-O-BENZYL-D-TYROSINE;N-ALPHA-TERT-BUTYLOXYCARBONYL-O-BENZYL-D-TYROSINE;BOC-D-TYROSINE(BZL)-OH;BOC-D-TYR(BZL)-OH;BOC-(R)-2-AMINO-3-(4'-BENZYLOXYPHENYL)PROPANOIC ACID;BOC-O-BENZYL-D-TYR;BOC-O-BENZYL-D-TYROSINE
    3. CAS NO:63769-58-4
    4. Molecular Formula: C21H25NO5
    5. Molecular Weight: 371.43
    6. EINECS: N/A
    7. Product Categories: Amino Acid Derivatives;Amino Acids
    8. Mol File: 63769-58-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 552.4 °C at 760 mmHg
    3. Flash Point: 287.9 °C
    4. Appearance: /Solid
    5. Density: 1.185g/cm3
    6. Vapor Pressure: 4.87E-13mmHg at 25°C
    7. Refractive Index: 1.562
    8. Storage Temp.: Store at RT.
    9. Solubility: N/A
    10. PKA: 2.99±0.10(Predicted)
    11. Water Solubility: Slightly soluble in water.
    12. CAS DataBase Reference: BOC-D-TYR(BZL)-OH(CAS DataBase Reference)
    13. NIST Chemistry Reference: BOC-D-TYR(BZL)-OH(63769-58-4)
    14. EPA Substance Registry System: BOC-D-TYR(BZL)-OH(63769-58-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 63769-58-4(Hazardous Substances Data)

63769-58-4 Usage

Chemical Properties

White to of-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 63769-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,6 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63769-58:
(7*6)+(6*3)+(5*7)+(4*6)+(3*9)+(2*5)+(1*8)=164
164 % 10 = 4
So 63769-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C21H25NO5/c1-21(2,3)27-20(25)22-18(19(23)24)13-15-9-11-17(12-10-15)26-14-16-7-5-4-6-8-16/h4-12,18H,13-14H2,1-3H3,(H,22,25)(H,23,24)/t18-/m1/s1

63769-58-4 Well-known Company Product Price

  • Brand
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  • Detail
  • Alfa Aesar

  • (H63427)  N-Boc-O-benzyl-D-tyrosine, 95%   

  • 63769-58-4

  • 1g

  • 250.0CNY

  • Detail
  • Alfa Aesar

  • (H63427)  N-Boc-O-benzyl-D-tyrosine, 95%   

  • 63769-58-4

  • 5g

  • 1873.0CNY

  • Detail
  • Alfa Aesar

  • (H63427)  N-Boc-O-benzyl-D-tyrosine, 95%   

  • 63769-58-4

  • 25g

  • 3756.0CNY

  • Detail

63769-58-4SDS

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 (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(4-phenylmethoxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names N-(tert-butoxycarbonyl)-D-(O-benzyl)tyrosine

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:63769-58-4 SDS

63769-58-4Relevant articles and documents

Approaches to the Synthesis of Endothiopeptides: Synthesis of a Thioamide-Containing C-Terminal Bombesin Nonapeptide

Jurayj, Jurjus,Cushman, Mark

, p. 8601 - 8614 (2007/10/02)

Several approaches have been investigated for the synthesis of a bombesin C-terminal nonapeptide analogue AsnGlnTrpAlaValGlyHisLeu-ΨCSNHMet-NH2.A new activated dithioester 16 has been synthesized.Thioacylation of methionine methyl ester with 16 was always

Design of more potent antagonists of the antidiuretic responses to arginine-vasopressin

Manning,Olma,Klis,Kolodziejczyk,Seto,Sawyer

, p. 45 - 50 (2007/10/02)

As part of a program aimed at designing more potent and selective antagonists of the antidiuretic responses to arginine-vasopressin (AVP), the authors substituted O-alkyl-D-tyrosine (where alkyl=methyl, ethyl, isopropyl, or n-propyl) at position 2 in our

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