101759-74-4

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• Basic information

  1. Product Name: N-Boc-(S)-2-(MethylaMino)butyric acid
  2. Synonyms: N-Boc-(S)-2-(MethylaMino)butyric acid;(S)-2-((tert-Butoxycarbonyl)(methyl)amino)butanoic acid
  3. CAS NO:101759-74-4
  4. Molecular Formula: C₁₀H₁₉NO₄
  5. Molecular Weight: 217.26216
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 101759-74-4.mol
  9. Article Data: 5

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 312.4±21.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.089±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: 2-8°C
  8. Solubility: N/A
  9. PKA: 4.01±0.10(Predicted)
  10. CAS DataBase Reference: N-Boc-(S)-2-(MethylaMino)butyric acid(CAS DataBase Reference)
  11. NIST Chemistry Reference: N-Boc-(S)-2-(MethylaMino)butyric acid(101759-74-4)
  12. EPA Substance Registry System: N-Boc-(S)-2-(MethylaMino)butyric acid(101759-74-4)

• 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: 101759-74-4(Hazardous Substances Data)

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• 101759-74-4

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• Suzhou Health Chemicals Co., Ltd.
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• Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]methylamino]...

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• Kono Chem Co.,Ltd
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• N-Boc-(S)-2-(MethylaMino)butyric acid

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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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• (S)-2-((tert-Butoxycarbonyl)(methyl)amino)butanoic acid

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• ENAO Chemical Co, Limited
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• N-Boc-(S)-2-(MethylaMino)butyric acid

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• Chemical Technology Co.,LTD
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• N-Boc-(S)-2-(methylamino)butyric acid

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101759-74-4 Usage

General Description

N-Boc-(S)-2-(MethylaMino)butyric acid is a chemical compound used in the synthesis of pharmaceuticals and biologically active molecules. It is a derivative of the amino acid alanine and contains a protected amine group and an N-terminal Boc (tert-butoxycarbonyl) protecting group. N-Boc-(S)-2-(MethylaMino)butyric acid has potential application in the development of new drugs and therapeutic agents due to its ability to modify and stabilize peptide structures. It is important for its role in peptide chemistry and drug discovery, and its incorporation into various molecules can lead to the creation of new pharmaceutical compounds with a range of therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 101759-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,7,5 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 101759-74:
(8*1)+(7*0)+(6*1)+(5*7)+(4*5)+(3*9)+(2*7)+(1*4)=114
114 % 10 = 4
So 101759-74-4 is a valid CAS Registry Number.

101759-74-4Upstream product

• 70606-05-2 D,L-N-Methyl-α-aminobuttersaeure 
• 24424-99-5 di-tert-butyl dicarbonate 
• 58632-95-4 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile 
• 34306-42-8 Boc-Abu 
• 74-88-4 methyl iodide 
• 124-38-9 carbon dioxide 
• 140150-48-7 Methyl-((R)-1-tributylstannanyl-propyl)-carbamic acid tert-butyl ester 

101759-74-4Downstream Products

• 1190769-02-8 C₃₄H₄₅N₇O₅ 
• 1151560-50-7 C₃₅H₄₅N₅O₅ 
• 1266230-43-6 C₃₅H₅₃N₅O₆ 

101759-74-4Relevant articles and documents

2-OXO-2,3,4,5-TETRAHYDRO-1 H-BENZO[B]DIAZEPINES AND THEIR USE IN THE TREATMENT OF CANCER

-

Paragraph 0371, (2015/09/22)

Disclosed are compounds of Formula I or pharmaceutically acceptable salts thereof, wherein W, Y, Z, R1, R2, R3, R4 and R5 are described herein, and methods of using said compounds in the treatment of cancer.

Peptide Enolates. C-Alkylation of Glycine Residues in Linear Tri-, Tetra-, and Pentapeptides via Dilithium Azadienediolates

Bossler, Hans G.,Seebach, Dieter

, p. 1124 - 1165 (2007/10/02)

The Boc-protected tripeptides Boc-Val-Gly-Leu-OH (1), Boc-Leu-Sar-Leu-OH (2), Boc-Leu-Gly-MeLeu-OH (3), and Boc-Val-BzlGly-Leu-OMe (64), tetrapeptide Boc-Leu-Gly-Pro-Leu-OH (9), and pentapeptides Boc-Val-Leu-Gly-Abu-Ile-OH (4), Boc-Val-Leu-Sar-MeAbu-Ile-O

Synthesis of new indolactam analogues by microbial conversion

Kajiyama, Shin-Ichiro,Irie, Kazuhiro,Kido, Takae,Koshimizu, Koichi,Hayashi, Hideo,Arai, Motoo

, p. 5453 - 5462 (2007/10/02)

Ten indolactam congeners with L-Ala, Abu, γ,δ-Δ-Nva, Nva, Nle, tert-Leu, Leu, Ile, allo-Ile. Phg instead ofL-Val in (-)-indolactam-Val, were synthesized from their seco-compounds (N-methyl-L-amino acidyl-L-tryptophonol) by microbial conversion.

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