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1145-56-8

1145-56-8

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1145-56-8 Usage

Chemical Properties

white fine powder

Check Digit Verification of cas no

The CAS Registry Mumber 1145-56-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1145-56:
(6*1)+(5*1)+(4*4)+(3*5)+(2*5)+(1*6)=58
58 % 10 = 8
So 1145-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H12ClNO4/c12-6-10(15)13-9(11(16)17)5-7-1-3-8(14)4-2-7/h1-4,9,14H,5-6H2,(H,13,15)(H,16,17)/p-1/t9-/m0/s1

1145-56-8 Well-known Company Product Price

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  • TCI America

  • (C0131)  N-Chloroacetyl-L-tyrosine  >98.0%(T)

  • 1145-56-8

  • 1g

  • 250.00CNY

  • Detail

  • TCI America

  • (C0131)  N-Chloroacetyl-L-tyrosine  >98.0%(T)

  • 1145-56-8

  • 5g

  • 850.00CNY

  • Detail

1145-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[(2-chloroacetyl)amino]-3-(4-hydroxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names N-Chloroacetyl-L-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:1145-56-8 SDS

1145-56-8Relevant articles and documents

PCl3-mediated synthesis of green/cyan fluorescent protein chromophores using amino acids

Singh, Thokchom Prasanta,Shunmugam, Raja

, p. 3024 - 3027 (2016)

Convenient synthesis involving aromatic amino acids, acetyl chlorides, and anilines in the presence of phosphorous trichloride has been established for the rapid synthesis of functionalized imidazolinones. With all the starting materials which are commercially available, low cost and stable, the construction of the target products has been accomplished via tandem transformations involving a key C-N coupling process, leading to the formation of two C(sp2)-N, one C=N, and one C=C bonds.

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