126587-35-7 Usage
General Description
(S)-Methyl 4-(tert-butoxycarbonylamino)-5-hydroxypentanoate is a chemical compound consisting of a hydroxy ester attached to a tert-butoxycarbonyl protected amino group. It is a chiral compound with a methyl group in the (S) configuration. (S)-METHYL 4-(TERT-BUTOXYCARBONYLAMINO)-5-HYDROXYPENTANOATE can be used in the synthesis of pharmaceuticals and other bioactive molecules. It possesses both ester and amino functionalities, making it a versatile building block for organic synthesis. The tert-butoxycarbonyl protecting group can be removed under mild conditions, revealing the amino function for further chemical manipulations. The hydroxy ester moiety can also participate in various organic transformations, making this compound a valuable intermediate in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 126587-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,8 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126587-35:
(8*1)+(7*2)+(6*6)+(5*5)+(4*8)+(3*7)+(2*3)+(1*5)=147
147 % 10 = 7
So 126587-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H21NO5/c1-11(2,3)17-10(15)12-8(7-13)5-6-9(14)16-4/h8,13H,5-7H2,1-4H3,(H,12,15)/t8-/m0/s1
126587-35-7Relevant articles and documents
TLR2 MODULATOR COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF
-
Paragraph 001011-001012, (2021/12/08)
The present disclosure relates to compounds which modulate the activity of Toll-like receptor (TLR) proteins, including agonists or activators, partial agonists, and antagonists. Of particular interest of compounds that modulate the activity of TLR2, as well as methods of using such compounds to treat cancer and other disorders associated with a TLR2 pathway.
Synthesis method of moCys section of marine natural product apratoxin E
-
Paragraph 0012, (2017/01/19)
The invention relates to a synthesis method of moCys section of a marine natural product apratoxin E, and belongs to the field of chemical synthesis. The moCys section (C27 to C30 section) of the marine natural product apratoxin E is prepared from cheap a
New approach toward the total synthesis of (+)-batzellaside B
Wierzejska, Jolanta,Motogoe, Shin-Ichi,Makino, Yuto,Sengoku, Tetsuya,Takahashi, Masaki,Yoda, Hidemi
, p. 1831 - 1838,8 (2020/09/16)
A new synthetic approach to (+)-batzellaside B from naturally abundant L-pyroglutamic acid is presented in this article. The key synthetic step involves Sharpless asymmetric dihydroxylation of an olefinic substrate functionalized with an acetoxy group to
