structure of Fmoc-Thr(tBu)-OH CAS 71989-35-0Custom Synthesis for Unnatural Amino Acids Iden­ti­fi­ca­tion Prop­er­ties Safe­ty Data Spec­i­fi­ca­tions and Oth­er Information Links

Iden­ti­fi­ca­tion

CAS Number

71989-35-0

Name

Fmoc-Thr(tBu)-OH

Syn­onyms

3,5-Dichlorbenzoesäure [Ger­man] [ACD/IUPAC Name] 3,5-Dichlorobenzoic acid [ACD/IUPAC Name] 3,5-Dichloro-benzoic acid 51-36-5 [RN] Acide 3,5-dichlorobenzoïque [French] [ACD/IUPAC Name] Ben­zoic acid, 3,5-dichloro- [ACD/​Index Name] QVR CG EG [WLN] [51-36-5] 200-092-4 [EINECS] 3,5-dichlorobenzoic_acid 71989-35-0 [RN] 75248-87-2 [RN] BR-47334 DG7350000 OS-1286

Mol­e­c­u­lar Structure

structure of Fmoc-Thr(tBu)-OH CAS 71989-35-0

struc­ture of Fmoc-Thr(tBu)-OH CAS 71989-35-0

SMILES

c1c(cc(cc1Cl)Cl)C(=O)O

Std­InChI

InChI=1S/C7H4Cl2O2/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3H,(H,10,11)

Std­InChIKey

CXKCZF­­DUOY­­MOOP-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C23H27NO5

Mol­e­c­u­lar Weight

397.47

EINECS

276-261-1

Beil­stein Reg­istry Number

4581133

MDL Number

MFCD00077075

Prop­er­ties

Appear­ance

Off-white to white pow­der

Melt­ing Point

125-135℃

Safe­ty Data

Sym­bol

exclamation-mark-jpg GHS09

Sig­nal Word

Warn­ing

Haz­ard Statements

H410

Pre­cau­tion­ary Statements

P273-P501

Per­son­al Pro­tec­tive Equipment

Eye­shields, Gloves, type N95 (US), type P1 (EN143) res­pi­ra­tor fil­ter

RIDADR

UN 3077 9 / PGI­II

WGK Germany

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our Fmoc-Thr(tBu)-OH CAS 71989-35-0

Stan­dard

Enter­prise Stan­dard.

Iden­ti­fi­ca­tion Methods

HNMR,HPLC

Puri­ty

98% min

Spe­cif­ic Rotation[a]20D

+16o±2 o (C=1 in EtOAc)

Loss on Drying

≤2.0% (60℃,2h)

IR Spectrum

In accor­dance with the stan­dard

Mass Spec­trum

In accor­dance with the stan­dard

NMR Spectrum

In accor­dance with the stan­dard

Ele­ment analysis(C、H、N)

≤5%

Clar­i­ty of solution

0.3 gram in 2ml DMF clear solu­tion

Kaiser Test

<0.05%

Water Content(K.F.)

≤1.0%

Stor­age

2-8 degrees Cel­sius away from light

Appli­ca­tion

Com­mon­ly used in pep­tide syn­the­sis, amino acids used as pro­tec­tion monomer

Links

This prod­uct is devel­oped by our RandD com­pa­ny Apnoke Sci­en­tif­ic Ltd(http://www.apnoke.com//), and here is the cor­re­spond­ing linkhttp://​apnoke​.com/​f​m​o​c​-​t​h​r​t​b​u​-​o​h​-​c​a​s​-​7​1​9​8​9​-​3​5​-0/

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