Structure of Fmoc Gly Gly Gly Gly CAS 1001202 16 9 - Fmoc-Gly-Gly-Gly-Gly CAS 1001202-16-9

Iden­ti­fi­ca­tion

CAS Number

1001202-16-9

Name

Fmoc-Gly-Gly-Gly-Gly

Syn­onyms

Glycine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycylglycylglycyl- [ACD/​Index Name]
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]glycylglycylglycylglycin [Ger­man] [ACD/IUPAC Name]
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]glycylglycylglycylglycine [ACD/IUPAC Name]
N-[(9H-Fluorén-9-ylméthoxy)carbonyl]glycylglycylglycylglycine [French] [ACD/IUPAC Name]
(((9H-fluoren-9-yl)methoxy)carbonyl)glycylglycylglycylglycine
[1001202-16-9]
{2-[2-(2-{[(9H-FLU­O­REN-9-YLMETHOXY)CAR­BONYL]AMINO}ACETAMI­DO)ACETAMI­DO]ACETAMI­DO}ACETIC ACID
1-(9H-Fluoren-9-yl)-3,6,9,12-tetraoxo-2-oxa-4,7,10,13-tetraazapentadecan-15-oic acid
1001202-16-9 [RN]
2-(2-(2-(2-(((9H-fluoren-9-yl)methoxy)carbonyl)acetamido)acetamido)acetamido)acetic acid
2-(2-{2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)acetamido]acetamido}acetamido)acetic acid
2-[[2-[[2-[[2-(9H-fluoren-9-ylmethoxycarbonylamino)acetyl]amino]acetyl]amino]acetyl]amino]acetic acid
9-flu­o­renyl­methoxy­car­bonyl[NHCH2CO]3glycine
Fmoc-Gly-Gly-Gly-Gly
MFCD18427731 [MDL num­ber]
n-((9h-fluoren-9-ylmethoxy)carbonyl)glycylglycylglycylglycine
N-{[(9H-Fluoren-9-yl)methoxy]carbonyl}glycylglycylglycylglycine
N-Fmoc-Gly-Gly-Gly-Gly-OH

SMILES

c1ccc2c(c1)-c3ccccc3C2COC(=O)NCC(=O)NCC(=O)NCC(=O)NCC(=O)O

Std­InChI

InChI=1S/C23H24N4O7/c28-19(24-10-20(29)26-12-22(31)32)9-25-21(30)11-27-23(33)34-13-18-16-7-3-1-5-14(16)15-6-2-4-8-17(15)18/h1-8,18H,9-13H2,(H,24,28)(H,25,30)(H,26,29)(H,27,33)(H,31,32)

Std­InChIKey

ZJOX­A­­CLWN­QEOCP-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C23H24N4O7

Mol­e­c­u­lar Weight

468.46

MDL Number

MFCD18427731

Prop­er­ties

Appear­ance

White pow­der

Safe­ty Data

WGK Germany

3

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our Fmoc-Gly-Gly-Gly-Gly CAS 1001202-16-9 

Iden­ti­fi­ca­tion Methods

HPLC

Puri­ty

98% min

Stor­age

Under room tem­per­a­ture away from light

Pro­duc­tiv­i­ty

kg scale

Known Appli­ca­tion

Used for syn­the­sis­Bi­valirudin and Dulaglutide.

This prod­uct is devel­oped by our R&D com­pa­ny Apnoke Sci­en­tif­ic Ltd(http://​www​.apnoke​.com/), and here is the cor­re­spond­ing linkhttp://​www​.apnoke​.com/​f​m​o​c​-​g​l​y​-​g​l​y​-​g​l​y​-​g​l​y​-​c​a​s​-​1​0​0​1​2​0​2​-​1​6​-9/

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