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218769-48-3

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218769-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 218769-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,7,6 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 218769-48:
(8*2)+(7*1)+(6*8)+(5*7)+(4*6)+(3*9)+(2*4)+(1*8)=173
173 % 10 = 3
So 218769-48-3 is a valid CAS Registry Number.

218769-48-3SDS

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

1.2 Other means of identification

Product number -
Other names L-Tyrosine,N-[(1,1-dimethylethoxy)carbonyl]-3-iodo-O-(phenylmethyl)

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:218769-48-3 SDS

218769-48-3Downstream Products

218769-48-3Relevant articles and documents

Scalable Synthesis of Mycocyclosin

Zhu, Xu,McAtee, Christopher C.,Schindler, Corinna S.

supporting information, p. 2862 - 2866 (2018/05/29)

We report herein the scalable total synthesis of the secondary metabolite, mycocyclosin, initially isolated from Mycobacterium tuberculosis. Mycocylosin bears a highly strained 3,3′-dityrosine biaryl system which arises biosynthetically from an intramolec

Total synthesis of nominal diazonamides - Part 1: Convergent preparation of the structure proposed for (-)-diazonamide A

Li, Jing,Jeong, Susan,Esser, Lothar,Harran, Patrick G.

, p. 4765 - 4770 (2007/10/03)

Unable to bear the weight of scrutiny, the original structure proposed for (-)diazonamide A (1) must be revised. A convergent, stereocontrolled total synthesis provided 1, which shows altered physical and spectroscopic characteristics relative to those of

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