1,2-⁽¹³⁾C₂ 2-(tert-butoxycarbonylamino)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145142-99-0

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Basic information
1. Product Name: 1,2-⁽¹³⁾C₂ 2-(tert-butoxycarbonylamino)acetic acid
2. Synonyms:
3. CAS NO:145142-99-0
4. Molecular Formula:
5. Molecular Weight: 177.163
6. EINECS: N/A
7. Product Categories: N/A
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: 1,2-⁽¹³⁾C₂ 2-(tert-butoxycarbonylamino)acetic acid(CAS DataBase Reference)
10. NIST Chemistry Reference: 1,2-⁽¹³⁾C₂ 2-(tert-butoxycarbonylamino)acetic acid(145142-99-0)
11. EPA Substance Registry System: 1,2-⁽¹³⁾C₂ 2-(tert-butoxycarbonylamino)acetic acid(145142-99-0)
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: 145142-99-0(Hazardous Substances Data)

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145142-99-0 Usage

Isotope labeling

Contains two carbon-13 atoms

Structure

Amino acid derivative
Tert-butoxycarbonyl (Boc) group attached to the amino group
Acetic acid moiety attached to the carboxyl group

Functional groups

Amino group (NH2)
Carboxyl group (COOH)
Tert-butoxycarbonyl (Boc) group (OC(CH3)3)

Molecular weight

Approximately 173.19 g/mol

Appearance

White crystalline solid

Solubility

Soluble in organic solvents like methanol, ethanol, and acetonitrile

Stability

Stable under normal conditions, sensitive to strong acids and bases

Applications

Isotope labeling studies
Organic synthesis research

Protective group

Tert-butoxycarbonyl (Boc) group temporarily masks reactive functional groups during synthesis

Cleavage

Boc group can be removed using trifluoroacetic acid (TFA) or hydrochloric acid (HCl) to reveal the free amino group

Synthesis

Prepared through the reaction of the corresponding amino acid with di-tert-butyl dicarbonate (Boc2O) or other Boc-protecting agents

Reactivity

Reacts with various reagents to form different derivatives, depending on the specific synthetic route

Safety precautions

Handle with care, use appropriate personal protective equipment (PPE), and follow proper disposal procedures for waste materials

Storage

Store in a cool, dry place, away from light and heat, and in a sealed container to prevent degradation or contamination

Check Digit Verification of cas no

The CAS Registry Mumber 145142-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,4 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 145142-99:
(8*1)+(7*4)+(6*5)+(5*1)+(4*4)+(3*2)+(2*9)+(1*9)=120
120 % 10 = 0
So 145142-99-0 is a valid CAS Registry Number.

145142-99-0Upstream product

145142-99-0Downstream Products

1356584-80-9 tert-butyl N-[2-[[(1R)-2-(3,5-dichloroanilino)-1-[⁽²⁾H₃]methyl-2-oxo-1-[[4-(trifluoromethoxy)phenyl]methyl]ethyl]amino]-2-oxo[⁽¹³⁾C₂]ethyl]carbamate

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