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4-amino-2,3-dihydroxy-N-[1-(8-hydroxy-1-oxo-3,4-dihydro-1H-isochromen-3-yl)-3-methylbutyl]-5-methylhexanamide (non-preferred name) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126262-07-5

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126262-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126262-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,2,6 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 126262-07:
(8*1)+(7*2)+(6*6)+(5*2)+(4*6)+(3*2)+(2*0)+(1*7)=105
105 % 10 = 5
So 126262-07-5 is a valid CAS Registry Number.

126262-07-5SDS

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 4-amino-2,3-dihydroxy-N-[1-(8-hydroxy-1-oxo-3,4-dihydroisochromen-3-yl)-3-methylbutyl]-5-methylhexanamide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:126262-07-5 SDS

126262-07-5Downstream Products

126262-07-5Relevant academic research and scientific papers

Concise synthesis of PM-94128 and Y-05460M-A

Enomoto, Masaru,Kuwahara, Shigefumi

, p. 7566 - 7569 (2009)

(Chemical Equation Presented) The enantioselective total synthesis of PM-94128, a potent cytotoxin of microbial origin, was accomplished by a concise nine-step sequence of reactions in 14% overall yield from N-Boc-L-leucine. The synthesis of Y-05460M-A, a

Application of Pd-Catalyzed C-H Alkylation Reaction in Total Syntheses of Twelve Amicoumacin-Type Natural Products

Wang, Hui-Hong,Li, Zhao,Feng, Yi-Yue,Yin, Gao-Feng,Shi, Tao,He, Dian,Wang, Xiao-Dong,Wang, Zhen

, p. 6956 - 6960 (2021)

Enantioselective total syntheses of 12 amicoumacin-type natural products are accomplished with a palladium(II)-catalyzed C-H alkylation as the key step to furnish the 3,4-dihydroisocoumarin scaffold. The target chemicals are assembled in a convergent prot

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