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128300-09-4

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128300-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128300-09-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,0 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 128300-09:
(8*1)+(7*2)+(6*8)+(5*3)+(4*0)+(3*0)+(2*0)+(1*9)=94
94 % 10 = 4
So 128300-09-4 is a valid CAS Registry Number.

128300-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(1S)-5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-(hydroxymethyl)-1,2-dihydro-3H-benz<e>indole

1.2 Other means of identification

Product number -
Other names (+)-(1S)-5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-(hydroxymethyl)-1,2-dihydro-3H-benz[e]indole

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:128300-09-4 SDS

128300-09-4Relevant articles and documents

CYTOTOXIC AGENTS

-

, (2022/02/09)

The present invention provides a compound of formula (I): (T-X4)p-B1-X3-A-X2-L-X1-AM or pharmaceutically acceptable salts, tautomers, stereoisomers or mixtures thereof; wherein AM is (AM1); (AM2); or (AM3); with the proviso that the compound of formula (I) contains at least one sigma hole group; and with the proviso that no more than one of A, B1 and T is a sigma hole group; and each sigma hole group is independently: (SH1); (SH2); (SH3); (SH4); (SH5); (SH6); (SH7); (SH8); (SH9); or (SH10).

Synthesis, biological evaluation, and live cell imaging of novel fluorescent duocarmycin analogs

Tietze, Lutz F.,Behrendt, Frank,Pestel, Galina F.,Schuberth, Ingrid,Mitkovski, Mi?o

, p. 2559 - 2570 (2013/01/16)

For a better understanding of the mode of action of duocarmycin and its analogs, the novel fluorescent duocarmycin derivatives 13-15 and 17b-19b were synthesized, and their bioactivity as well as their cellular uptake investigated using confocal laser sca

Resolution of a CBI precursor and incorporation into the synthesis of (+)-CBI, (+)-CBI-CDPI1, (+)-CBI-CDPI2: Enhanced functional analogs of (+)-CC-1065. A critical appraisal of a proposed relationship between electrophile reactivity,

Boger,Ishizaki

, p. 793 - 796 (2007/10/02)

Details of the resolution of an immediate CBI precursor, (+)- and (-)-8, and its subsequent incorporation into (+)- and (-)-CBI-CDPI(n), optically-active enhanced functional analogs of (+)-CC-1065, are described. In marked contrast to a previously detaile

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