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56976-06-8

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  • L-Cysteine,N-[(1,1-dimethylethoxy)carbonyl]-S-(1,1-dimethylethyl)-, compd. withN-cyclohexylcyclohexanamine (1:1)

    Cas No: 56976-06-8

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56976-06-8 Usage

Chemical Properties

White to off-white powder

Uses

Boc-Cys(tBu)-OH, is a Cystine derivative, used in various chemical synthesis and peptide chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 56976-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,7 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56976-06:
(7*5)+(6*6)+(5*9)+(4*7)+(3*6)+(2*0)+(1*6)=168
168 % 10 = 8
So 56976-06-8 is a valid CAS Registry Number.

56976-06-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-S-tert-butyl-L-cysteine

1.2 Other means of identification

Product number -
Other names (2R)-3-tert-butylsulfanyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic 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:56976-06-8 SDS

56976-06-8Relevant articles and documents

Cysteine-based fluorescence "turn-on" sensors for Cu2+and Ag+

Haridas,Praveen Kumar,Suresh, Cherumuttathu H.

, p. 56539 - 56542 (2015/02/18)

We designed and synthesized twometal ion binding molecules 3a and 3b based on cysteine. In 3a, pyrene is used as a fluorescent probe, while 3b contains tryptophan, which acts as a fluorescent probe as well as facilitates metal ion binding. Detailed spectroscopic, calorimetric, microscopic and computational studies revealed the binding mode and the plausible structures of the complexes.

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