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63519-99-3

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63519-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63519-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,1 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63519-99:
(7*6)+(6*3)+(5*5)+(4*1)+(3*9)+(2*9)+(1*9)=143
143 % 10 = 3
So 63519-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C50H70N10O16S2/c1-7-15-35-47(69)73-23-37(59-49(71)75-21-33-17-11-9-12-18-33)43(65)53-30(4)42(64)58-40(26-78-28-52-32(6)62)46(68)56-36(16-8-2)48(70)74-24-38(60-50(72)76-22-34-19-13-10-14-20-34)44(66)54-29(3)41(63)57-39(45(67)55-35)25-77-27-51-31(5)61/h9-14,17-20,29-30,35-40H,7-8,15-16,21-28H2,1-6H3,(H,51,61)(H,52,62)(H,53,65)(H,54,66)(H,55,67)(H,56,68)(H,57,63)(H,58,64)(H,59,71)(H,60,72)

63519-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-[6,19-bis(acetamidomethylsulfanylmethyl)-9,22-dimethyl-2,5,8,11,15,18,21,24-octaoxo-25-(phenylmethoxycarbonylamino)-3,16-dipropyl-1,14-dioxa-4,7,10,17,20,23-hexazacyclohexacos-12-yl]carbamate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:63519-99-3 SDS

63519-99-3Relevant articles and documents

SYNTHESIS OF DES-N-TETRAMETHYLTRIOSTIN A FROM C-TERMINAL Z-D-SERINE TETRA- AND OCTADEPSIPEPTIDE INTERMEDIATES

Dhaon, Madhup K.,Gardner, Joseph H.,Olsen, Richard K.

, p. 57 - 62 (2007/10/02)

Des-N-tetramethyltriostin A (1), a known DNA-intercalation agent, has been synthesized from tetra- and octapeptide intermediates that have Z-D-serine at the C-terminal position.The procedure thus allows the fragment coupling and cyclization reactions lead

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