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trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121056-95-9 Structure
  • Basic information

    1. Product Name: trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate
    2. Synonyms: trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate
    3. CAS NO:121056-95-9
    4. Molecular Formula:
    5. Molecular Weight: 297.245
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121056-95-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate(121056-95-9)
    11. EPA Substance Registry System: trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate(121056-95-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 121056-95-9(Hazardous Substances Data)

121056-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121056-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,0,5 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 121056-95:
(8*1)+(7*2)+(6*1)+(5*0)+(4*5)+(3*6)+(2*9)+(1*5)=89
89 % 10 = 9
So 121056-95-9 is a valid CAS Registry Number.

121056-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (±)-Boc-α-phosphonoglycine trimethyl ester

1.2 Other means of identification

Product number -
Other names (+/-)-Boc-α-phosphonoglycine trimethyl ester

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:121056-95-9 SDS

121056-95-9Downstream Products

121056-95-9Relevant articles and documents

Synthesis of the octahydroindole unit of aeruginosins via asymmetric hydrogenation of the Diels-Alder adducts of 2-amido-2,4-pentadienoate

Hoshina, Yoichiro,Doi, Takayuki,Takahashi, Takashi

, p. 12740 - 12746 (2007)

An optically active octahydroindole, the core unit of aeruginosins (Choi) was synthesized. The Diels-Alder reaction of Danishefsky's diene with methyl (Z)-2-acetamido-2,4-pentadienoates provided the adducts regioselectively in good yield. The adducts were

Preparation method of Wittig-Horner reagent

-

Paragraph 0030-0032; 0041-0042, (2021/07/31)

A preparation method of a Wittig-Horner reagent is disclosed. According to the preparation method of the Wittig-Horner reagent provided by the invention, a compound with a structure as shown in a formula (I) and a glyoxylic acid aqueous solution with a sp

SYNTHESIS OF (S)-6-HYDROXYTRYPTOPHAN AND DERIVATIVES THEREOF

-

, (2020/07/07)

The present invention relates to novel methods and compounds for synthesizing amanitin derivatives. The invention in particular relates to methods for synthesizing (S)-6-hydroxy-tryptophan derivatives which can be used as building blocks for synthesizing

PEPTIDE NUCLEIC ACID MONOMERS AND OLIGOMERS

-

, (2017/07/06)

The invention relates to new peptide nucleic acid monomers and peptide nucleic acid oligomers comprising a dialkylamine side chain substituted with phosphonic acid ester group(s) or phosphonic acid group(s), and to the uses thereof.

A new convenient synthesis of N-acyl-2-(dimethoxyphosphoryl)glycinates

Mazurkiewicz, Roman,Ku?nik, Anna

, p. 3439 - 3442 (2007/10/03)

Easily accessible N-acyl-2-triphenylphosphonioglycinate tetrafluoroborates react smoothly with trimethylphosphite in the presence of methyltriphenylphosphonium iodide to give N-acyl-2-(dimethoxyphosphoryl)glycinates in good or very good yields. The dimeth

METHODS OF PREPARATION OF DEHYDRO-DIKETOPIPERAZINES IN LIQUID PHASE OR OF SOLID SUPPORTED PHASE

-

Page 7, (2008/06/13)

The preparation of any compound of the generic structure (I); wherein: R1 and R2 are substituents described in the main text. Cycl- is a group represented by either of the formulae (a) and (b); wherein: R3 to R8

Total synthesis of isoroquefortine C

Schiavi, Bruno M.,Richard, David J.,Joullie, Madeleine M.

, p. 620 - 624 (2007/10/03)

A short and efficient total synthesis of isoroquefortine C, the 3,12-(Z)-isomer of roquefortine C, from L-tryptophan methyl ester hydrochloride and 4(5)-(hydroxy)methylimidazole hydrochloride is described.

Carbacyclic peptide mimetics as VCAM-VLA-4 antagonists

Tilley, Jefferson,Kaplan, Gerry,Fotouhi, Nader,Wolitzky, Barry,Rowan, Karen

, p. 1163 - 1165 (2007/10/03)

Substitution of carbon for sulfur in a potent 13-membered cyclic disulfide containing peptide was accomplished via an intramolecular Wittig reaction and resulted in a series of 'carba' analogues. Potency in the VCAM-VLA-4 assay was sensitive to ring size and lower than that of the parent disulfide. (C) 2000 Elsevier Science Ltd. All rights reserved.

Synthesis of non-natural O-glycosylamino acids derived from n-pentenyl glycosides; model studies and proof of principle for glycopeptide synthesis

Allen, Jennifer R.,Danishefsky, Samuel J.

, p. 736 - 744 (2007/10/03)

Model studies on the transformation of the olefinic unit contained in n-pentenyl glycosides (NPGs) to glycoamino acids is described. The methodology involves a Horner-Emmons olefination with a protected glycine derived phosphonate, followed by asymmetric

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